New utilities of amide compounds

ABSTRACT

Compounds having an activity to enhance the expression of apoAI are provided, which are used as medicaments. 
     Compounds of formula (I): 
     
       
         
         
             
             
         
       
     
     in which ring A and Ar 1  are independently a monocyclic or bicyclic aromatic carbocyclic group or aromatic heterocyclic group, each of which may be optionally substituted, or the like; R is a hydrogen or the like; Z is oxygen or the like; Y 1  and Y 2  are a hydrogen, a lower alkyl, or the like; n is an integer of 0 to 2; the broken line is the presence or absence of a bond; and the wavy line represents a cis- or trans-geometrical isomerism with respect to the double bond; are disclosed.

FIELD OF THE INVENTION

This invention relates to a method for enhancing the expression of apolipoprotein AI, and novel compounds therefor.

BACKGROUND ART

Cholesterol is well known as a main etiologic factor for arteriosclerosis that causes severe heart diseases. Especially, increased levels of serum low density lipoprotein (LDL) are believed to be a definite risk factor for coronary heart diseases (CHDs). Remedies for decreasing the level of LDL-cholesterol (LDL-C) in plasma by use of statins have been shown to be clinically effective in preventing the onset of CHDs and improving the conditions of CHDs and survivals in patients suffering from hypercholesterolemia. However, about 40% of CHDs patients have a normal level of LDL-C, and are not always cured effectively by remedies for decreasing the level of LDL-C. On the other hand, it has been known that a half of CHDs patients having a normal level of LDL-C shows a lower level of high density lipoprotein (HDL) cholesterol (HDL-C).

Recently, the lower level of serum HDL-C has been shown to be an additional risk factor of the onset and the recurrence of CHD.

HDL plays an important role in reverse cholesterol transport system that is known as a biological mechanism to transfer an excess cholesterol in cells back to liver so as to maintain the level of cholesterol in living bodies normally.

Lipoproteins such as HDL is mainly comprised of lipids and proteins called apoprotein, and HDL comprises an apoprotein as referred to apolipoprotein AI (hereinafter, made up by apoAI) as a main component.

Excess free cholesterols (FCs) and phospholipids in peripheral cells are extracted by free apoAI to form lipoproteins called preβ-HDL(s). The excess FCs integrated in the preβ-HDLs are transformed into cholesteryl esters (CEs) by lecithin:cholesterol acyl transferase (LCAT), while the preβ-HDLs increase in their particle size to mature into spherical HDLs (HDL3s). The matured HDLs are classified into diverse subfractions based on the density, and these particles further grow up to form HDL2(s). CEs are continuously transferred into very low density lipoprotein (VLDL) and LDL by means of cholesterol ester-transporter protein (CETP). Those lipoproteins that integrate CEs are finally taken into the liver via receptors. During the course, apoAI is regenerated, and again interacts with peripheral cells to repeat the extraction of cholesterols and the regeneration of preβ-HDLs.

It has been well understood that HDL plays a central role in reverse cholesterol transport system and is a defensive factor of arteriosclerosis. It is expected that agents that promote the HDL functions could be clinically effective as medicaments for treating arteriosclerotic diseases. Accordingly, studies to develop agents that enhance the level of HDL in plasma have been conducted via various approaches.

Among them, one of the most promising approaches is to enhance the serum level of apoAI, a main component of HDL. It is understood that apoAI production increased by enhancing the expression of apoAI gene leads to directly the elevation of HDL-C level in plasma, resulting in the activation of reverse cholesterol transport system. In fact, it has been demonstrated that the mRNA level of apoAI in liver correlates closely with the levels of apoAI and HDL-C in blood (Dueland S., France D., Wang S L., Trawick J D., and Davis R A., J. Lipid Res., 38:1445-53 (1997), “Cholesterol 7alpha-hydroxylase influences the expression of hepatic apoA-I in two inbred mouse strains displaying different susceptibilities to atherosclerosis and in hepatoma cells.”). In addition, it has been shown that apoAI-transgenic mice and rabbit pathologic models administered with apoAI exhibit anti-arteriosclerosis activities (Rubin E. M., Krauss R. M., Spangler E. A., Verstuyft J. G., and Clift S. M., Nature 353, 265-267 (1991), “Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI.”; Plump A. S., Scott C. J., Breslow J. L., Proc. Natl. Acad. Sci. USA., 91, 9607-9611 (1994), “Human apolipoprotein A-I gene expression increases high density lipoprotein and suppress atherosclerosis in the apolipoprotein E-deficient mouse.”; Miyazaki A., Sakuma S., Morikawa W., Takiue T., Miake F., Terano T., Sakai M., Hakamata H., Sakamoto Y., et al., Arterioscler. Thromb. Vasc. Biol., 15, 1882-1888 (1995), “Intravenous injection of rabbit apolipoprotein A-I inhibits the progression of atherosclerosis in cholesterol-fed rabbits.”).

All those facts clearly suggest that agents that enhance the expression of apoAI would be candidates for medicaments of dyslipidemia, arteriosclerotic diseases, and other diverse diseases associated with HDL.

Compounds similar to the compounds according to the invention in terms of chemical structure are described in GB2327675, WO99/07669, WO99/24404, U.S. Pat. No. 5,670,066, DE19734438, Japanese Patent Publication (kokai) No. 41118/1994, Japanese Patent Publication (kokai) No. 14568/1991, Japanese Patent Publication (kokai) No. 253974/1992, Japanese Patent Publication (kokai) No. 147874/1999, and Journal of Pharmaceutical Sciences vol. 68, No. 7, 827-832, but the activities of these compounds are quite different from the activities according to the present invention.

Several compounds that have a chemical structure similar to the compounds of the invention, and that are described to be effective in treatment of hyperlipidemia, arteriosclerosis, and visceral fat syndrome have been known. Japanese Patent Publication (kokai) No. 68592/1991 describes the compounds that lower the level of triglycerides in plasma and consequently enhance the level of HDL-C, but the effect is caused by activating lipoprotein lipases (Goto, K., Nakamura, S., Morioka, Y., Kondo, M., Naito, S., Tsutsumi, K., Chem. Pharm. Bull., 44, 547-551 (1996), “Synthesis and Biological Activity of the Metabolites of Diethyl 4-[(4-Bromo-2-cyanophenyl)carbamoyl]-benzylphosphonate (NO-1886)”). WO98/39280 and WO98/02412 describe the compounds that inhibit acyl-CoA cholesterol acyltransferase (ACAT) thereby suppressing the accumulation of cholesterol in macrophage. Japanese Patent Publication (kokai) No. 171848/1999 describes the compounds that inhibit acetyl-CoA carboxylase thereby suppressing the biosynthesis of triglycerides. WO99/07382 describes the compounds that have an antagonist activity of macrophage scavenger receptors. Japanese Patent Publication (kokai) No. 158133/1999 describes the compounds that have activities for suppressing LDL oxidation and inhibiting ACAT. As described above, the known compounds are quite different from the compounds of the invention in terms of action mechanism.

Compounds that increase apoAI are described in Japanese Patent Publication (kokai) No. 221959/1993, Japanese Patent Publication (kokai) No. 291094/1996, and WO97/09048, but those compounds are different from the compounds of the invention in chemical structure.

DISCLOSURE OF THE INVENTION

The present invention is directed to methods for enhancing the expression of apoAI, and novel compounds having the activity thereof.

Specifically, the invention provides

1) A method of enhancing the expression of apoAI, which comprises administrating a therapeutically effective amount of a compound of formula (I):

in which

ring A is Ar² or a group of

Ar¹ and Ar² are independently a monocyclic or bicyclic aromatic carbocyclic group that may be optionally substituted, or a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted;

ring B is a monocyclic non-aromatic carbocyclic group that may be optionally substituted, or a monocyclic non-aromatic heterocyclic group that may be optionally substituted;

R is a hydrogen or a lower alkyl that may be optionally substituted;

Z is oxygen or sulfur;

Y¹ and Y² are independently a hydrogen, a halogen, a lower alkyl that may be optionally substituted, a carboxy, a lower alkoxycarbonyl that may be optionally substituted, a cyano, a phenyl that may be optionally substituted, or a monocyclic aromatic heterocyclic group that may be optionally substituted, and two Y's or more and two Y²S or more each may be different among them;

n is an integer of 0 to 2;

the broken line is independently the presence or absence of a bond; and

the wavy line represents a cis- or trans-geometrical isomerism with respect to the double bond; a prodrug thereof, a pharmaceutically acceptable salt or solvate of them to a patient expected to enhance the expression of apoAI;

2) The method according to above 1), in which Ar¹ in formula (I) is a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted, and that contains a nitrogen atom at the position adjacent to the constituent atom of the ring that has a binding bond; 3) The method according to above 1), in which Ar¹ in formula (I) is 2-pyridyl, 2-quinolyl, 2-quinoxalyl, 2-benzisoxazolyl, 2-benzothiazolyl, or 2-benzimidazolyl, each of which may be optionally substituted; 4) The method according to any one of above 1) to 3), in which Ar² in formula (I), which is condensed with ring B, is a benzene ring that may be optionally substituted, or a monocyclic aromatic heterocyclic group that may be optionally substituted; 5) The method according to any one of above 1) to 3), in which ring A in formula (I) is a phenyl that may be optionally substituted, or a monocyclic aromatic heterocyclic group that may be optionally substituted; 6) The method according to above 5), in which ring A in formula (I) is a phenyl or a monocyclic aromatic heterocyclic group, each of which may be optionally substituted, wherein the substituent is a halogen; a lower alkyl optionally substituted by a halogen or a lower alkoxy; a hydroxy; a lower alkoxy; phenoxy; naphthyloxy; an acyloxy; a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl or a lower acyl; a phenyl that may be optionally substituted by a lower alkoxy; a nitro; a lower alkylthio; a cyano; a monocyclic heterocyclic group; or an alkylenedioxy; 7) The method according to any one of above 1) to 6), in which Y¹ and/or Y² in formula (I) is a hydrogen; 8) The method according to any one of above 1) to 7), in which Z in formula (I) is oxygen; 9) The method according to any one of above 1) to 8), in which n in formula (I) is 1 or 2, and all of the broken line are the presence of a bond; 10) The method according to above 9), in which when n is 1 and the broken line is the presence of a bond, then the wavy line represents trans configuration with respect to the relationship between NRCZ and ring A, or alternatively when n is 2 and the broken lines are the presence of a bond, then the wavy line represents trans configuration with respect to the relationship between NRCZ and CY² and/or the relationship between CY¹ and ring A; 11) A method of treatment or prevention of dyslipidemia or arteriosclerotic diseases, which comprises administrating a therapeutically effective amount of a compound of formula (I) as defined in above 1), a prodrug thereof, a pharmaceutically acceptable salt or solvate of them to a patient suspected to have dyslipidemia or arteriosclerotic diseases; preferably the method thereof which comprises administrating a therapeutically effective amount of the compound as defined in any one of above 2) to 10), a prodrug thereof, a pharmaceutically acceptable salt or solvate of them; 12) A compound of formula (II):

in which

Het¹ is pyridyl, furyl, 3-thienyl or pyrrolyl;

R is a hydrogen, or a lower alkyl;

W¹ is CR³ or N; and

R¹, R², R³, R⁴ and R⁵ are independently a hydrogen, a hydroxy, a lower alkyl, a lower alkoxy, a carboxy, a lower alkoxycarbonyl, an amino, a lower alkylamino, or an acyl; a prodrug thereof, a pharmaceutically acceptable salt or solvate of them;

13) A compound of formula (III):

in which

Het² is pyridyl, furyl, thienyl or pyrrolyl;

R is a hydrogen, or a lower alkyl that may be optionally substituted;

W² is CR⁸ or N;

Y¹ and Y² are independently a hydrogen, a halogen, a lower alkyl that may be optionally substituted, a carboxy, a lower alkoxycarbonyl that may be optionally substituted, a cyano, a phenyl that may be optionally substituted, or a monocyclic aromatic heterocyclic group that may be optionally substituted;

R⁶, R⁷, R⁸, R⁹ and R¹⁰ are independently a hydrogen, a halogen, a hydroxy, a lower alkyl that may be optionally substituted, a lower alkoxy that may be optionally substituted, a carboxy, a lower alkoxycarbonyl that may be optionally substituted, an amino that may be optionally substituted, or an acyl that may be optionally substituted;

any two of R⁶, R⁷, and R⁸ may be combined to form a cyclic ring group;

m is 1 or 2;

the broken line is independently the presence or absence of a bond; and

the wavy line represents a cis- or trans-geometrical isomerism with respect to the double bond; a prodrug thereof, a pharmaceutically acceptable salt or solvate of them;

14) The compound according to above 13), in which W² is CH; R is a hydrogen or a lower alkyl, and all of the broken line are the presence of a bond; a prodrug thereof, a pharmaceutically acceptable salt or solvate of them;

15) A pharmaceutical composition, which comprises the compound according to any one of above 12) to 14), a prodrug thereof, a pharmaceutically acceptable salt or solvate of them, together with a pharmaceutically acceptable additive; 16) The pharmaceutical composition according to above 15), which is used to enhance the expression of apoAI; and 17) The pharmaceutical composition according to above 15), which is used for prevention and/or treatment of dyslipidemia or arteriosclerotic diseases.

Further, the invention provides a method of enhancing the expression of apoAI, and a method of prevention or treatment of dyslipidemia or arteriosclerotic diseases, both of which comprises administrating a therapeutically effective amount of a compound of formula (II) or (III) as described above: a prodrug thereof, a pharmaceutically acceptable salt or solvate of them.

As used herein, each two Y¹s and Y²s as resulted from the case that n is 2 may be different each other.

The term “halogen” as used herein includes fluorine, chlorine, bromine and iodine.

The term “lower alkyl” as used herein refers to a straight or branched chain alkyl comprising 1 to 6 carbon atoms, preferably 1 to 3 carbon atoms. Examples of the lower alkyl include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, hexyl, isohexyl, and the like.

The term “lower alkyl that may be optionally substituted” as used herein includes a lower alkyl, of which any position may be substituted by one or more substituents. The substituent includes a halogen, a hydroxy, a lower alkoxy, a monocyclic or bicyclic carbocyclic group, an acyl, an acyloxy, a carboxy, a lower alkoxycarbonyl, an amino, a lower alkylamino, a nitro, a monocyclic or bicyclic heterocyclic group, and the like.

Alkyl moiety of “lower alkoxy”, “lower alkylthio” or “lower alkylamino” is similar to the “lower alkyl” as described above.

The term “alkylenedioxy” specifically includes methylenedioxy, ethylenedioxy, and the like.

Substituent in “lower alkoxy that may be optionally substituted” is similar to the substituent of “lower alkyl that may be optionally substituted” as described above.

Lower alkyl moiety of “lower alkoxycarbonyl” is similar to the “lower alkyl” as described above, and substituent of “lower alkoxycarbonyl that may be optionally substituted” is similar to the substituent of “lower alkyl that may be optionally substituted” as described above.

The term “acyl” includes an aroyl and an aliphatic acyl containing 1 to 7 carbon atoms. Here, “aroyl” refers to a group wherein a carbonyl group is bonded to an aromatic carbocyclic group or an aromatic heterocyclic group. Examples of the acyl include formyl, acetyl, propionyl, butyryl, isobutyryl, valery, pivaloyl, hexanoyl, acryloyl, propioloyl, methacryloyl, crotonoyl, and benzoyl. Acyl moiety of “acyloxy” is similar to the “acyl”.

Substituent of “acyl that may be optionally substituted” is similar to the substituent of the “lower alkyl that may be optionally substituted” as described above, and the aroyl may be substituted by a lower alkyl. Acyl may be substituted at one or more arbitrary positions by such a substituent.

The term “amino that may be optionally substituted” includes an unsubstituted, mono-substituted, or di-substituted amino. Examples of the substituents include the substituents of the “lower alkyl that may be optionally substituted” as described above.

The term “monocyclic non-aromatic carbocyclic group” as used herein refers to a cyclic ring group containing 3 to 10 carbon atoms, preferably 5 to 8 carbon atoms, and includes a non-aromatic cyclic group that may contain one or more double bond at any position. Examples includes cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, cycloheptenyl, cycloheptadienyl, cyclooctyl, cyclooctenyl, cyclooctadienyl, cyclononyl, and cyclodecyl.

The term “monocyclic carbocyclic group” as used herein refers to a cyclic ring group containing 3 to 10 carbon atoms, preferably 5 to 8 carbon atoms, and includes “monocyclic non-aromatic carbocyclic group” as described above, and a phenyl.

The term “monocyclic aromatic carbocyclic group” as used herein refers to a phenyl (or a benzene ring).

The term “monocyclic aromatic heterocyclic group” refers to an aromatic heterocyclic group containing one or more hetero atoms selected from the group consisting of N, S and O within its ring. Examples include pyrrolyl, imidazolyl, pyrazolyl, pyridyl, pyridazinyl, pyrimidyl, pyrazinyl, triazolyl, triazinyl, tetrazolyl, isoxazolyl, oxazolyl, oxadiazolyl, isothiazolyl, thiazolyl, thiadiazolyl, furyl, and thienyl.

The term “monocyclic non-aromatic heterocyclic group” refers to a non-aromatic cyclic group wherein one or more carbon atoms that are contained in the “monocyclic non-aromatic carbocyclic group” as described above, and that can be substituted, are substituted by a hetero atom selected from the group consisting of N, S and O. Examples include dioxanyl, dioxazinyl, dioxolanyl, dioxolyl, dithiazinyl, imidazolidinyl, imidazolinyl, morpholyl, oxazinyl, oxadiazyl, furazaryl, oxathianyl, oxathiazinyl, oxathiolanyl, oxazolidinyl, oxazolinyl, piperazinyl, piperidinyl, pyranyl, pyrazolidinyl, pyrazolinyl, pyrrolidinyl, pyrrolinyl, tetrahydropyranyl, thiadiazolidinyl, thianyl, thiazinyl, thiadiazinyl, thiiranyl, and thiolanyl.

The term “monocyclic heterocyclic group” includes “monocyclic aromatic heterocyclic group” and “monocyclic non-aromatic heterocyclic group” as described above, and include preferably pyridyl, pyrimidinyl, pyrrolyl, furyl, thienyl, and thiazolyl.

Heterocyclic moiety of “monocyclic aromatic heterocyclic oxy” is similar to the aromatic heterocyclic group as described above.

The term “bicyclic carbocyclic group” refers to an aromatic or non-aromatic cyclic group containing 6 to 12 carbon atoms wherein two cyclic rings are condensed. Examples include naphthyl, indanyl, indenyl, dihydronaphthyl, and tetrahydronaphthyl, and preferably, naphthyl.

The term “bicyclic aromatic carbocyclic group” refers to naphthyl (or a naphthalene ring).

The term “bicyclic heterocyclic group” includes a cyclic ring compound wherein one or more carbon atoms that are contained in the “bicyclic carbocyclic group” as described above, and that can be substituted, are substituted by a hetero atom selected from the group consisting of N, S and O. Examples include aromatic heterocyclic groups such as indolyl, isoindolyl, indolizinyl, benzimidazolyl, indazolyl, cinnolinyl, phthalazinyl, benzoxazolyl, benzisoxazolyl, benzoxadiazolyl, benzothiazolyl, benzisothiazolyl, benzothiadiazolyl, benzofuryl, isobenzofuryl, benzothienyl, benzotriazolyl, imidazopyridyl, triazolopyridyl, imidazothiazolyl, pyrazinopyridazinyl, quinazolinyl, quinolyl, isoquinolyl, quinoxalinyl, purinyl, pteridinyl, naphthylidinyl, and pyrazinopyridazinyl, and non-aromatic heterocyclic groups such as chromanyl, 2H-chromenyl, coumarinyl, coumaranonyl, 1,3-dioxaindanyl, indolinyl, isoindolinyl, dihydroquinolyl, dihydroisoquinolyl, tetrahydroquinolyl, tetrahydroisoquinolyl, 6,7-dihydro-5H-[1]pyrimidinyl, benzothiazinyl, tetrahydroquinoxalyl, cyclopentenopyridinyl, 4,5,6,7-tetrahydro-1H-indolyl, 4-oxochromenyl, 3,4-dihydro-2H-benzo[1,4]oxazinyl, and pyrrolidinyl. Preferable examples include indolyl, benzimidazolyl, benzoxazolyl, benzoxadiazolyl, benzothiazolyl, benzothiadiazolyl, benzofuryl, benzothienyl, imidazopyridyl, triazolopyridyl, quinolyl, isoquinolyl, and quinoxalinyl.

The term “bicyclic aromatic heterocyclic group” refers to only an aromatic heterocyclic group among the groups of “bicyclic heterocyclic group” as described above.

Substituent in “monocyclic or bicyclic carbocyclic group that may be optionally substituted”, “monocyclic carbocyclic group that may be optionally substituted”, “phenyl that may be optionally substituted”, and “monocyclic or bicyclic aromatic carbocyclic group that may be optionally substituted” includes a halogen; a hydroxy; a lower alkyl optionally substituted by a halogen, a hydroxy, or a lower alkoxy; a lower alkoxy optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkenyl optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkenyloxy optionally substituted by a halogen or a hydroxy; a lower alkylthio; a non-aromatic carbocyclic group optionally substituted by a halogen, a hydroxy, or a lower alkyl; an acyl; an acyloxy; a carboxy; a lower alkoxycarbonyl; a lower alkenyloxycarbonyl; an amino optionally substituted by a lower alkyl or an acyl; a hydrazino, a nitro; a cyano; a monocyclic or bicyclic aromatic carbocyclic group optionally substituted by a halogen, a hydroxy, a lower alkyl, or a lower alkoxy; a monocyclic or bicyclic heterocyclic group; a phenoxy optionally substituted by a halogen, a hydroxy, or a lower alkyl; a monocyclic aromatic heterocyclic oxy; an oxo; and an alkylenedioxy, all of which may be bonded at one or more arbitrary positions.

Preferable examples include a halogen; a hydroxy; a lower alkyl optionally substituted by a halogen or a hydroxy; a lower alkoxy optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkenyl optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkylthio; an acyl; an acyloxy; a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl or an acyl; a hydrazino, a nitro; a cyano; a phenyl; a monocyclic or bicyclic heterocyclic group; an oxo; and an alkylenedioxy.

Substituent in “monocyclic aromatic heterocyclic group that may be optionally substituted”, “monocyclic non-aromatic heterocyclic group that may be optionally substituted”, “monocyclic heterocyclic group that may be optionally substituted”, “monocyclic aromatic heterocyclic group that may be optionally substituted”, “monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted”, “2-pyridyl that may be optionally substituted”, and “2-pyridyl, 2-quinolyl, 2-quinoxalyl, 2-benzisoxazolyl, 2-benzothiazolyl, or 2-benzimidazolyl, each of which may be optionally substituted” is similar to the substituent in “monocyclic or bicyclic carbocyclic group that may be optionally substituted” and the like as described above. Preferable examples include a halogen; a hydroxy; a lower alkyl optionally substituted by a lower alkoxy; a lower alkoxy; a lower alkenyl; a lower alkylthio; an acyl; an acyloxy; a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl; and a phenyl and a monocyclic heterocyclic group optionally substituted by a lower alkoxy.

The term “a monocyclic or bicyclic aromatic heterocyclic group that contains a nitrogen atom at the position adjacent to the constituent atom of the ring that has a binding bond” includes “a monocyclic or bicyclic aromatic heterocyclic group” as described above that has a binding bond to NRCZ at ortho position with respect to the N atom that constitutes a ring. Specific examples include monocyclic aromatic heterocyclic groups such as 2-pyridyl, 2- or 4-pyrimidinyl, 3-pyridazinyl, 2-pyrazinyl, 1,3,5-triazin-2-yl, 2-pyrrolyl, 1- or 3-pyrazolyl, 2- or 4-imidazolyl, 2- or 4-oxazolyl, 3-isoxazolyl, 1,3,4-oxadiazol-2-yl, 1,3-thiazol-2-yl, 1,3-thiazol-4-yl, 1,2,5-thiadiazol-3-yl, 1,2,3-thiadiazol-4-yl, 1,3,4-thiadiazol-2-yl, 3-isothiazolyl, 1,2,3-triazol-4-yl, 1H-tetrazol-1-yl, and 1H-tetrazol-5-yl; and bicyclic aromatic heterocyclic groups such as 2-benzimidazolyl, 3-benzisothiazolyl, 3-benzisoxazolyl, 2-benzoxazolyl, 2-benzothiazolyl, 1-benzotriazolyl, 1- or 3-indazolyl, 3-cinnolinyl, 2-indolyl, 1- or 3-isoindolyl, 2-naphthylidinyl, 2-, 4-, 6- or 7-pteridinyl, 2-, 6 or 8-purinyl, 1- or 3-isoquinolyl, 2-quinolyl, 2- or 4-quinazolinyl, and 2-quinoxalinyl. Those substituents may be bonded at one or more arbitrary positions similarly to “monocyclic or bicyclic carbocyclic group that may be optionally substituted” as described above.

The phrase “any two of R⁶, R⁷, and R⁸ are combined to form a cyclic ring group” means that any two of R⁶, R⁷, and R⁸ are combined with a constituent atom of a pyridine or pyrimidine ring to which they are bonded to form a non-aromatic carbocyclic group, a benzene ring, or a heterocyclic group. Specific examples include quinolyl, isoquinolyl, quinazolinyl, pteridinyl, purinyl, pyridoxazinyl, tetrahydroquinolyl, tetrahydroisoquinolyl, or tetrahydroquinazolinyl.

A group of the formula:

refers to a bicyclic or tricyclic group, preferably a bicyclic group, which is formed by condensing ring B with Ar². Ring B means a 4- to 7-membered non-aromatic carbocyclic group or non-aromatic heterocyclic group, which may contain one or more double bonds at any position. A constituent atom of ring B and Ar² may be carbon, nitrogen, oxygen, or sulfur.

Preferable ring B includes a moiety of the formula:

wherein W³ is CR¹¹R¹², O, NR¹³, or S;

R¹¹, R¹², and R¹³ are independently a hydrogen, a halogen, a hydroxy; a lower alkyl optionally substituted by a halogen or a hydroxy; a lower alkoxy optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkenyl optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkylthio; an acyl; an acyloxy; a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl or an acyl; a hydrazino, a nitro; a cyano; a phenyl; or a heterocyclic group; and R¹¹ and R¹² may be combined to form an oxo; and

the broken line is the presence or absence of a bond.

Examples of Ar² to be condensed with ring B include a benzene ring. In this case, specific examples of ring A include 1-, 2-, 3- or 4-dihydronaphthalenyl, 1-, 2- or 3-indolinyl, 1- or 2-indanyl, 1-, 2- or 3-indenyl, 1- or 2-tetrahydronaphthalenyl, 2-, 3- or 4-1,2-dihydroquinolinyl, 3- or 4-isochromanyl, 2-, 3- or 4-chromanyl, 2-, 3- or 4-chromenyl, 2-, 3- or 4-thiochromenyl, 2-, 3- or 4-benzothiopyranyl, 2- or 3-dihydrobenzothienyl, 2- or 3-dihydrobenzofuryl, 2-benzo[1,3]dioxolyl, 2-2,3-dihydrobenzo[1,4]dioxonyl, 2- or 3-3,4-dihydro-2H-benzo[1,4]oxadinyl, 8- or 9-6,7-dihydro-5H-benzocycloheptenyl, and 2-, 3- or 4-oxo-4H-chromenyl.

In addition to a benzene ring, example of Ar² to be condensed with ring B include 6-membered cyclic groups such as pyridine, pyrazine, and pyrimidine; 5-membered cyclic groups such as pyrrole, furan, thiophene, oxazole, isoxazole, and thiazole; and bicyclic aromatic cyclic groups such as quinoline, isoquinoline, and indole, all of which may be replaced for a benzene contained in the examples of ring A as described above.

Ring B and Ar² may be substituted by a substituent at any position which is similar to those of a monocyclic or bicyclic carbocyclic group that may be optionally substituted.

The compounds according to the invention include pharmaceutically acceptable, producible salts. Examples of the “pharmaceutically acceptable salts” include a salt with an inorganic acid e.g. those with hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, or the like; a salt with an organic acid e.g. those with p-toluenesulfonic acid, methanesulfonic acid, oxalic acid, citric acid, or the like; a salt with an organic base e.g. ammonium, trimethylammonium, triethylammonium, or the like; a salt with an alkaline metal e.g. sodium, potassium, or the like; a quaternary salt with alkyl halide e.g., methyl iodide, ethyl iodide or the like; and a salt with an alkaline earth metal e.g., calcium, magnesium, or the like.

The compounds according to the invention may form solvates as coordinated with a suitable organic solvent and/or water. Hydrates are exemplified.

The compounds according to the invention also include prodrugs. In the context of the invention, a “prodrug” is a derivative of a compound according to the invention comprising a chemically or metabolically cleavable group. In the course of metabolism in the body, a prodrug shows a pharmacological activity as a result of conversion to the compounds according to the invention. Method for selecting and producing suitable prodrug derivatives are described in, e.g. “Design of Prodrugs, Elsevier, Amsterdam (1985)”.

Prodrugs of a compound according to the invention having a carboxy are exemplified by an ester derivative prepared by condensing the carboxy group with a suitable alcohol, and alternatively by an amide derivative prepared by reacting the carboxy and a suitable amine.

Prodrugs of a compound according to the invention having a hydroxy are exemplified by an acyloxy derivative prepared by reacting the hydroxy group and a suitable acyl halide or a suitable acid anhydride.

Prodrugs of a compound according to the invention having an amino are exemplified by an amide derivative prepared by reacting the amino group and a suitable acid halide or a suitable mixed anhydride compound.

When compound (I) according to the invention has asymmetric carbon atom(s), then the invention encompasses a racemate, both of enantiomers, and all of diastereomers. When compound (I) according to the invention has a double bond, the invention includes both of geometric isomers resulting from possible arrangements of its substituents.

Although all of the compounds according to the invention have an activity for enhancing the expression of apoAI, the following compounds can be listed as preferable compounds. In formula (I):

1) a compound wherein Ar¹ is a monocyclic or bicyclic aromatic carbocyclic group that may be optionally substituted, or a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted wherein the substituent is a halogen; a lower alkyl optionally substituted by a halogen; a hydroxy; a lower alkoxy; an aryloxy; an acyloxy; a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl or a lower acyl; a phenyl; a nitro; a lower alkylthio; a cyano; a monocyclic heterocyclic group; or an alkylenedioxy (hereinafter, Ar¹ is regarded as Ar1-a);

a compound wherein Ar¹ is a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted, and that contains a nitrogen atom at the position adjacent to the constituent atom of the ring that has a binding bond wherein the substituent is similar to those in Ar1-a (hereinafter, Ar¹ is regarded as Ar1-b);

a compound wherein Ar¹ is a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted by a lower alkyl or an amino, and that contains a nitrogen atom at the position adjacent to the constituent atom of the ring that has a binding bond (hereinafter, Ar¹ is regarded as Ar1-c);

a compound wherein Ar¹ is an unsubstituted monocyclic or bicyclic aromatic heterocyclic group, and that contains a nitrogen atom at the position adjacent to the constituent atom of the ring that has a binding bond (hereinafter, Ar¹ is regarded as Ar1-d);

a compound wherein Ar¹ is 2-quinolyl, 2-quinoxalyl, 2-benzimidazolyl, 2-thiazolyl, 2-benzothiazolyl, 2-oxazolyl, 2-benzoxazolyl, 2-oxadiazolyl, 2-pyridyl, 2-pyrimidyl, or 2-imidazolyl (hereinafter, Ar¹ is regarded as Ar1-e);

2) a compound wherein ring A is a monocyclic or bicyclic aromatic carbocyclic group that may be optionally substituted, or a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted wherein the substituent is a halogen; a lower alkyl optionally substituted by a halogen; a hydroxy; a lower alkoxy; an aryloxy; an acyloxy, a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl or a lower acyl; a phenyl; a nitro; a lower alkylthio; a cyano; a monocyclic heterocyclic group; or an alkylenedioxy (hereinafter, ring A is regarded as A-a);

a compound wherein ring A is a monocyclic or bicyclic aromatic carbocyclic group that may be optionally substituted, or a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted wherein the substituent is a halogen; a lower alkyl optionally substituted by a halogen; an acyloxy; a lower alkoxy; an alkylenedioxy; or a phenyl (hereinafter, ring A is regarded as A-b);

a compound wherein ring A is a monocyclic or bicyclic aromatic heterocyclic group that is not substituted (hereinafter, ring A is regarded as A-c);

a compound wherein ring A is a phenyl, 2-naphthyl, 2- or 3-furyl, 2- or 3-thienyl, 2- or 3-pyrrolyl, 2-, 3- or 4-pyridyl, 2-indolyl, 2-benzofuryl, 6-quinolyl, 2- or 6-benzothienyl, or 3-2H-chromenyl (hereinafter, ring A is regarded as A-d);

a compound wherein ring A is a group of the formula:

and Ar² is A-a (hereinafter, ring A is regarded as A-e);

a compound wherein ring A is a group of the formula:

and Ar² is A-b (hereinafter, ring A is regarded as A-f);

a compound wherein ring A is a group of the formula:

and Ar² is A-c (hereinafter, ring A is regarded as A-g);

a compound wherein ring A is a group of the formula:

and Ar² is benzene, pyridine, pyrazine, pyrimidine, pyrrole, furan, thiophene, oxazole, isoxazole, thiazole, quinoline, isoquinoline, or indole, and ring B is a moiety of the formula:

wherein W³ is CR¹¹R¹², O, NR¹³, or S;

R¹¹, R¹², and R¹³ are independently a hydrogen, a halogen, a hydroxy; a lower alkyl optionally substituted by a halogen or a hydroxy; a lower alkoxy optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkenyl optionally substituted by a halogen, a hydroxy, a carboxy, or a lower alkoxycarbonyl; a lower alkylthio; an acyl; an acyloxy; a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl or an acyl; a hydrazino, a nitro; a cyano; a phenyl; or a heterocyclic group; and

the broken line is the presence or absence of a bond (hereinafter, ring A is regarded as A-h);

3) a compound wherein R is a hydrogen; 4) a compound wherein Z is oxygen; 5) a compound wherein Y¹ and Y² are independently a hydrogen, a halogen, a lower alkyl or a cyano (hereinafter, Y¹ and Y² are regarded as Y-a);

a compound wherein Y¹ and Y² are independently a hydrogen, or a lower alkyl (hereinafter, Y¹ and Y² are regarded as Y-b);

a compound wherein Y¹ and Y² are a hydrogen (hereinafter, Y¹ and Y² are regarded as Y-c);

6) a compound wherein n is 1 or 2, and all of the broken line are the presence of a bond;

a compound wherein n is 1, and the broken line is the presence of a bond;

7) a compound wherein R is a hydrogen, Z is oxygen, n is 0, and a combination of Ar¹ and ring A (Ar1, A) is as follows: (Ar1, A)=(Ar1-a, A-a), (Ar1-a, A-b), (Ar1-a, A-c), (Ar1-b, A-a), (Ar1-b, A-b), (Ar1-b, A-c), (Ar1-c, A-a), (Ar1-c, A-b), (Ar1-c, A-c), (Ar1-d, A-a), (Ar1-d, A-b), (Ar1-d, A-c), (Ar1-e, A-a), (Ar1-e, A-b), (Ar1-e, A-c), (Ar1-a, A-e), (Ar1-a, A-f), (Ar1-a, A-g), (Ar1-b, A-e), (Ar1-b, A-f), (Ar1-b, A-g), (Ar1-c, A-e), (Ar1-c, A-f), (Ar1-c, A-g), (Ar1-d, A-e), (Ar1-d, A-f), (Ar1-d, A-g), (Ar1-e, A-d), (Ar1-e, A-e), (Ar1-e, A-f), (Ar1-e, A-g), (Ar1-e, A-h); 8) a compound wherein R is a hydrogen, Z is oxygen, n is 1 or 2, the broken line is the presence of a bond, and a combination of Ar¹, Y¹ and Y², and ring A (Ar1, Y, A) is as follows: (Ar1, Y, A)=(Ar1-a, Y-c, A-a), (Ar1-a, Y-c, A-b), (Ar1-a, Y-c, A-c), (Ar1-b, Y-c, A-a), (Ar1-b, Y-c, A-b), (Ar1-b, Y-c, A-c), (Ar1-c, Y-c, A-a), (Ar1-c, Y-c, A-b), (Ar1-c, Y-c, A-c), (Ar1-d, Y-c, A-a), (Ar1-d, Y-c, A-b), (Ar1-d, Y-c, A-c), (Ar1-e, Y-c, A-a), (Ar1-e, Y-c, A-b), (Ar1-e, Y-c, A-c), (Ar1-e, Y-c, A-d), (Ar1-e, Y-c, A-h) (Ar1-a, Y-b, A-a), (Ar1-a, Y-b, A-b), (Ar1-a, Y-b, A-c) (Ar1-b, Y-b, A-a), (Ar1-b, Y-b, A-b), (Ar1-b, Y-b, A-c), (Ar1-c, Y-b, A-a), (Ar1-c, Y-b, A-b), (Ar1-c, Y-b, A-c), (Ar1-d, Y-b, A-a), (Ar1-d, Y-b, A-b), (Ar1-d, Y-b, A-c), (Ar1-e, Y-b, A-a), (Ar1-e, Y-b, A-b), (Ar1-e, Y-b, A-c), (Ar1-a, Y-c, A-e), (Ar1-a, Y-c, A-f), (Ar1-a, Y-c, A-g), (Ar1-b, Y-c, A-e), (Ar1-b, Y-c, A-f), (Ar1-b, Y-c, A-g), (Ar1-c, Y-c, A-e), (Ar1-c, Y-c, A-f), (Ar1-c, Y-c, A-g), (Ar1-d, Y-c, A-e), (Ar1-d, Y-c, A-f), (Ar1-d, Y-c, A-g), (Ar1-e, Y-c, A-e), (Ar1-e, Y-c, A-f), (Ar1-e, Y-c, A-g), (Ar1-a, Y-b, A-e), (Ar1-a, Y-b, A-f), (Ar1-a, Y-b, A-g), (Ar1-b, Y-b, A-e), (Ar1-b, Y-b, A-f), (Ar1-b, Y-b, A-g), (Ar1-c, Y-b, A-e), (Ar1-c, Y-b, A-f), (Ar1-c, Y-b, A-g), (Ar1-d, Y-b, A-e), (Ar1-d, Y-b, A-f), (Ar1-d, Y-b, A-g), (Ar1-e, Y-b, A-e), (Ar1-e, Y-b, A-f), (Ar1-e, Y-b, A-g), ; and a prodrug thereof, a pharmaceutically acceptable salt or solvate of them.

More preferable compounds are exemplified by the following, which are described in the examples: Ia-1, Ia-3, Ia-4, Ia-5, Ia-6, Ia-7, Ia-9, Ia-10, Ia-16, Ia-17, Ia-18, Ia-23, Ia-27, Ia-29, Ia-30, Ia-37, Ia-38, Ia-39, Ia-42, Ia-44, Ia-45, Ia-46, Ia-48, Ia-53, Ia-54, Ia-55, Ia-59, Ia-60, Ia-61, Ia-62, Ia-63, Ia-64, Ia-69, Ia-72, Ia-95, Ia-97, Ia-104, Ia-105, Ia-112, Ia-113, Ia-118, Ia-119, Ia-144, Ia-145, Ia-146, Ia-150, Ia-152, Ia-153, Ia-156, Ia-161, Ia-162, Ia-177, Ia-204, Ib-01, Ib-3, Ib-4, Ib-6, Ib-7, Ib-8, Ib-9, Ib-11, Ib-12, Ib-13, Ib-14, Ib-144, Ib-17, Ib-18, Ib-19, Ib-20, Ib-24, Ib-25, Ib-26, Ib-28, Ib-35, Ib-73, Ib-97, Ib-102, Ib-105, Ib-131, Ib-137, Id-1, and Id-11.

BEST MODE FOR CARRYING OUT THE INVENTION

Compounds (I) of the invention may be synthesized for example according to Method A to C. Hereinafter, an illustrative preparation is described. Detailed are referred to example in Synthetic Organic Chemistry VI, Japan, 4 (1977) 6, 79, or The 4th series of experimental chemistry (1992) 22, 138.

Method A: A-1+A-2→I

in which Hal is a halogen, and other symbols are as defined above.

The process involves a reaction between amines (A-1) and acid halides (A-2), which leads to compounds (I) in a conventional manner. In general, the reaction may be conducted in the presence of base, e.g., triethylamine, pyridine, excess of (A-1), or dimethylaminopyridine in methylene chloride or tetrahydrofuran as a solvent. The reaction may proceed at a temperature between an ice-cooling and a reflux temperature of the solvent.

Method B: B-1+B-2→I

in which the symbols are as defined above.

The process is also a conventional synthesis of amides. In the reaction, amines (B-1) and carboxylic acids (B-2) are directly condensed in the presence of a condensing agent such as dicyclohexylcarbodiimide or 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride to give compounds (I′). The reaction may proceed in a solvent such dimethylformamide, methylene chloride or tetrahydrofuran at a temperature between room temperature and a reflux temperature of the solvent.

Method C: C-1+C-2→I

in which the symbols are as defined above.

The process also involves a condensation reaction between amines (C-1) and carboxylic acids (C-2), which may be conducted according to the method as described in Eur. J. Med. Chem., (1994) 29, 841. Specifically, carboxylic acid (C-2) is activated by triphenylphosphine and bromotrichloromethane, and the activated acid is reacted with an amine to give compounds (I′). The reaction may proceed in a solvent such methylene chloride or tetrahydrofuran at a temperature between room temperature and a reflux temperature of the solvent.

Compound (I) wherein R is H as obtained by the method described above may be reacted with a alkyl halide in the presence of sodium hydride in dimethylformamide at a temperature between room temperature to 80° C. to give compound (I) wherein R is a lower alkyl.

Compound (I) wherein Z is sulfur may be obtained by heating compound (I) wherein Z is oxygen in the presence of phosphorus pentasulfide or Lawesson's reagent in a solvent such as pyridine or toluene at a reflux temperature of the solvent.

The method of enhancing the expression of apoAI according to the invention activates a reverse cholesterol transport activity of HDL, an anti-inflammatory activity and an anti-coagulant activity, or the like. As a result, the method of the invention are useful for preventing and/or treating dyslipidemia, arteriosclerotic diseases and various cardiovascular diseases concomitant with them, which are caused by decreased level of HDL in serum. “Dyslipidemia” specifically include conditions of lowered level of serum HDL, hypercholesteremia and hypertriglyceridemia; “arteriosclerotic diseases” specifically include arteriosclerosis, myocardial infarction, and cardiac incompetence; and “various cardiovascular diseases associated with the above diseases” include hyperuricemia, coronary artery diseases, ischaemic heart diseases, corneal opacity, cerebrovascular disease, and hereditary HDL deficiencies (Tangier disease, fish-eye disease).

When a compound of the invention is administered in the method according to the invention, pharmaceutical compositions therefor may be administered either orally or parenterally. For oral routes, the compositions may be formulated conventionally into usual dosage forms such as tablets, tablets, granules, powders, capsules, pills, solutions, syrups, buccals, sublinguals, or the like before administration. For parenteral administration, the compositions may be conventionally formulated into usual dosage forms such as injections, e.g., intramuscular or intravenous injections, suppositories; transdermal patches, inhalation, or the like.

An effective amount of a compound according to the invention may be admixed with various suitable pharmaceutical additives such as excipient, binding agent, wetting agent, disintegrating agent, lubricant, diluent, or the like to give pharmaceutical compositions, if necessary. In the case of injections, the ingredients are sterilized together with a suitable carrier to formulate the composition.

More specifically, the excipients include lactose, sucrose, glucose, starch, calcium carbonate, crystalline cellulose, or the like; the binding agents include methyl cellulose, carboxymethylcellulose, hydroxypropylcellulose, gelatine, polyvinyl pyrrolidone, or the like; the disintegrating agents include carboxymethylcellulose, sodium carboxymethyl cellulose, starch, sodium alginate, algae powder, sodium lauryl sulfate, or the like; the lubricants include talc, magnesium stearate or Macrogol, or the like. Base materials of the suppository may be for example cacao butter, Macrogol, methylcellulose, or the like. Solutions, emulsions or suspensions for injection may comprise a solubilizing agent, a suspending agent, an emulsifying agent, a stabilizing agent, a preserving agent, an isotonic agent, or the like as usually used. Compositions for oral administration may comprise a flavoring agent, an aromatic agent, or the like.

Dose or therapeutically effective amount of the compounds according to the invention for enhancing the expression of apoAI is preferably determined considering age and body weight of patients, sort and severity of diseases to be treated, route of administration, or the like. In the case of oral administration to an adult, the dose range is usually 1 to 100 mg/kg/day, preferably 5 to 30 mg/kg/day. In the case of parenteral administration, the dose differs largely depending on the route of administration, but the dose range is usually 0.1 to 10 mg/kg/day, preferably 1 to 5 mg/kg/day. The dosage unit may be administered to a subject once or several times per day.

Following examples and experiments are presented for purpose of further illustration of the invention, and they are not intended to limit the scope of the invention in any respect.

EXAMPLE 1 4-Chloro-N-(4-tolyl)benzamide (Ib-17)

Method A: To a solution of p-toluidine (1.07 g, 10.0 mmol) in chloroform (20 ml) were added pyridine (2.37 g, 30.0 mmol) and then p-chlorobenzoyl chloride (2.63 g, 15.0 mmol) under ice-cooling, and the mixture was stirred at room temperature for 5 hours. After water was added to the reaction, the precipitated solids were collected by filtration, washed sequentially with aqueous saturated sodium hydrogen carbonate, water and chloroform, and then recrystallized from acetone to give Ib-17 (2.0 g, 81.6%).

EXAMPLE 2 Thiophen-2-caroxypyridin-2-yl amide (Ib-122)

Method C: To a solution of 2-aminopyridine (376 mg, 3.99 mmol), triphenylphosphine (786 mg, 3.00 mmol) and bromotrichloromethane (990 mg, 4.99 mmol) in tetrahydrofuran (10 ml) was added 2-thiophen carboxylic acid (256 mg, 2.00 mmol), and the mixture was heated at reflux for 6 hours, after which the solvent was removed in vacuo. The residue was subjected to silica gel chromatography using ethyl acetate-hexane=1:3 as eluent to give crystals, which were recrystallized from 95% ethanol to give Ib-122 (342 mg, 83.8%).

EXAMPLE 3 N-Methyl-N-phenylbenzamide (Ib-27)

A solution of Ib-1 (180 mg, 0.91 mmol) in dimethylformamide (3 ml) was dropwise added to sodium hydride (60%, 40 mg, 1.00 mmol) under ice-cooling, and the mixture was stirred at room temperature for 30 minutes. To the mixture was added methyl iodide (213 mg, 1.50 mmol), and the reaction was allowed to proceed for 5 hours. After an ice water was added to the reaction, the mixture was extracted with ethyl acetate, and then the extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo. The residue was subjected to silica gel chromatography using ethyl acetate-hexane=1:1 as eluent to give Ib-27 (180 mg, 85.3%) as colorless oil.

EXAMPLE 4 3-Phenyl-N-quinoxalin-2-yl-acrylamide (Ia-9)

Method A: To a solution of 2-aminoquinoxaline (435 mg, 3.00 mmol) in tetrahydrofuran (12 ml) were added triethylamine (728 mg, 7.20 mmol) and cinnamoyl chloride (1.20 g, 7.20 mmol) with stirring under ice-cooling, and the reaction was continued for 5 hours, after which the mixture was allowed to stand overnight. After an ice water was added to the reaction, the mixture was extracted with ethyl acetate, and then the extract was washed with water, and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo. The residue was subjected to silica gel chromatography using ethyl acetate-hexane=1:2 as eluent, followed by recrystallization from ethyl acetate-hexane to give Ia-9 (128 mg, 15.5%).

EXAMPLE 5 3-Pyridin-3-yl-N-pyridin-2-yl-acrylamide (Ia-112)

Method B: To a solution of 2-aminopyridine (0.986 g, 10.48 mmol) and β-(3-pyridyl)acrylic acid (0.746 g, 5.00 mmol) in tetrahydrofuran (10 ml) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.006 g, 5.25 mmol), and the mixture was stirred for 21 hours, then the solvent was removed in vacuo. To the residue was added a 10% citric acid aqueous solution, and the mixture was extracted with chloroform. The extract was washed with water, aqueous saturated sodium hydrogen carbonate and water, dried over anhydrous magnesium sulfate. The solvent was removed in vacuo. The residue was purified by silica gel chromatography using ethyl acetate-hexane=1:1, followed by recrystallization from ethyl acetate-chloroform (1:1) to give Ia-112 (440 mg, 39.0%).

EXAMPLE 6 3-Furan-2-yl-N-pyridin-2-yl-acrylamide (Ia-104)

Method C: To a solution of 2-aminopyridine (376 mg, 4.00 mmol), triphenylphosphine (786 mg, 3.00 mmol) and bromotrichloromethane (990 mg, 4.99 mmol) in tetrahydrofuran (10 ml) was added 2-furan acrylic acid (276 mg, 2.00 mmol), and the mixture was heated at reflux for 6 hours, after which the solvent was removed in vacuo. The residue was subjected to silica gel chromatography using ethyl acetate-hexane=1:2 as eluent to give crystals, which were then recrystallized from 95% ethanol to give Ia-104 (243 mg, 56.8%).

In a similar manner, other compounds were prepared, of which chemical structures are shown in the following tables

TABLE 1 Ia

No. Ar¹ A Ia-1 

Ia-2 

Ia-3 

Ia-4 

Ia-5 

Ia-6

Ia-7 

Ia-8 

Ia-9 

Ia-10

Ia-11

Ia-12

Ia-13

Ia-14

Ia-15

Ia-16

Ia-17

Ia-18

Ia-19

Ia-20

Ia-21

Ia-22

Ia-23

Ia-24

Ia-25

IA-26

Ia-27

Ia-28

Ia-29

Ia-30

Ia-31

Ia-32

Ia-33

Ia-34

Ia-35

Ia-36

TABLE 2 Ia

No. Ar¹ A Ia-37

Ia-38

Ia-39

Ia-40

Ia-41

Ia-42

Ia-43

Ia-44

Ia-45

Ia-46

Ia-47

Ia-48

Ia-49

Ia-50

Ia-51

Ia-52

Ia-53

Ia-54

Ia-55

Ia-56

Ia-57

Ia-58

Ia-59

Ia-60

Ia-61

Ia-62

Ia-63

Ia-64

Ia-65

Ia-66

Ia-67

Ia-68

TABLE 3 Ia

No. Ar¹ A Ia-69

Ia-70

Ia-71

Ia-72

Ia-74

Ia-75

Ia-76

Ia-77

Ia-78

Ia-79

Ia-80

Ia-81

Ia-82

Ia-83

Ia-84

Ia-85

Ia-86

Ia-87

Ia-88

Ia-89

Ia-90

Ia-91

Ia-92

Ia-93

Ia-94

Ia-95

Ia-96

Ia-97

Ia-98

Ia-99

 Ia-100

 Ia-101

 Ia-102

 Ia-103

TABLE 4 Ia

No. Ar¹ A Ia-104

Ia-105

Ia-106

Ia-107

Ia-108

Ia-109

Ia-110

Ia-111

Ia-112

Ia-113

Ia-114

Ia-115

Ia-116

Ia-117

Ia-118

Ia-119

Ia-120

Ia-121

Ia-122

Ia-123

Ia-124

Ia-125

Ia-126

Ia-127

Ia-128

Ia-129

Ia-130

Ia-131

Ia-132

Ia-133

Ia-134

Ia-135

Ia-136

Ia-137

Ia-138

Ia-139

Ia-140

Ia-141

Ia-142

Ia-143

TABLE 5 Ia

No. Ar¹ A Ia-144

Ia-145

Ia-146

Ia-147

Ia-148

Ia-149

Ia-150

Ia-151

Ia-152

Ia-153

Ia-154

Ia-155

Ia-156

Ia-157

Ia-158

Ia-159

Ia-160

Ia-161

Ia-162

Ia-163

Ia-164

Ia-165

Ia-166

Ia-167

Ia-168

Ia-169

Ia-170

Ia-171

Ia-172

Ia-173

Ia-174

Ia-175

TABLE 6 Ia

No. Ar¹ A Ia-176

Ia-177

Ia-178

Ia-179

Ia-180

Ia-181

Ia-182

Ia-183

Ia-184

Ia-185

Ia-186

Ia-187

Ia-188

Ia-189

Ia-190

Ia-191

Ia-192

Ia-193

Ia-194

Ia-195

Ia-196

Ia-197

Ia-198

Ia-199

Ia-200

Ia-201

Ia-202

Ia-203

Ia-204

Ia-205

Ia-206

Ia-207

Ia-208

Ia-209

TABLE 7 Ib

R No. Ar¹ (*1) A Ib-1 

Ib-2 

Ib-3 

Ib-4 

Ib-5 

Ib-6 

Ib-7 

Ib-8 

Ib-9 

Ib-10

Ib-11

Ib-12

Ib-13

Ib-14

Ib-15

Ib-16

Ib-17

Ib-18

Ib-19

Ib-20

Ib-21

Ib-22

Ib-23

Ib-24

Ib-25

Ib-26

Ib-27

Me

Ib-28

Ib-29

Ib-30

Ib-31

Ib-32

(*1) R is H unless otherwise noted

TABLE 8 Ib

No. Ar¹ R (*1) A Ib-33

Ib-34

Ib-35

Ib-36

Ib-37

Ib-38

Ib-39

Ib-40

Ib-41

Ib-42

Ib-43

Ib-44

Ib-45

Ib-46

Ib-47

Ib-48

Ib-49

Ib-50

Ib-51

Ib-52

Ib-53

Ib-54

Ib-55

Ib-56

Ib-57

Ib-58

Ib-59

Ib-60

Ib-61

Ib-62

Ib-63

(*1) R is H unless otherwise noted

TABLE 9 Ib

No. Ar¹ R (*1) A Ib-64

Ib-65

Ib-66

Ib-67

Ib-68

Ib-69

Ib-70

Ib-71

Ib-72

Ib-73

Ib-74

Ib-75

Ib-76

Ib-77

Ib-78

Ib-79

Ib-80

Ib-81

Ib-82

Ib-83

Ib-84

Ib-85

Me

Ib-86

Ib-87

Ib-88

Ib-89

Et

Ib-90

Ib-91

Ib-92

Ib-93

Ib-94

Ib-95

Ib-96

(*1) R is H unless otherwise noted

TABLE 10 Ib

No. Ar¹ R (*1) A Ib-97 

Ib-98 

Ib-99 

Ib-100

Ib-101

Ib-102

Ib-103

Ib-104

Ib-105

Ib-106

Ib-107

Ib-108

Ib-109

Ib-110

Et

Ib-111

Ib-112

Ib-113

Ib-114

Ib-115

Ib-116

Ib-117

Ib-118

Ib-119

Me

Ib-120

Ib-121

Ib-122

Ib-123

Ib-124

Ib-125

Ib-126

Ib-127

Ib-128

Ib-129

(*1) R is H unless otherwise noted

TABLE 11 Ib

No. Ar¹ R (*1) A Ib-130

Ib-131

Ib-132

Ib-133

Ib-134

Ib-135

Ib-136

Ib-137

Ib-138

Me

Ib-139

Ib-140

Ib-141

Ib-142

Ib-143

Ib-144

Ib-145

Ib-146

Ib-147

Ib-148

Ib-149

Ib-150

Ib-151

Ib-152

Ib-153

Me

Ib-154

Ib-155

Ib-156

Ib-157

Ib-158

Ib-159

Ib-160

Ib-161

Ib-162

Ib-163

(*1) R is H unless otherwise noted

TABLE 12 Ib

R No. Ar¹ (*1) A Ib-164

Ib-165

Ib-166

Ib-167

Et

Ib-168

Ib-169

Ib-170

Ib-171

Ib-172

Ib-173

Ib-174

Ib-175

Ib-176

Ib-177

Ib-178

Ib-179

Ib-180

Ib-181

Ib-182

Ib-183

Ib-184

Ib-185

Ib-186

Ib-187

Ib-188

Ib-189

Ib-190

Ib-191

Ib-192

(*1) R is H unless otherwise noted

TABLE 13 Ic

Dashed No. Ar¹ A lines Bond Ic-1

cis presence Ic-2

cis presence Ic-3

cis presence Ic-4

cis presence Ic-5

absence Id

No. Ar¹ A Id-1

Id-2

Id-3

Id-4

Id-5

Id-6

Id-7

Id-8

Id-9

 Id-10

TABLE 14 m.p Molecular Elemental analysis Elemental analysis Compound (° C.) formula (Calculated) (Found) NMR Ia-1 153-155 C15H13NO C, 80.69, H, 5.87; C, 80.86; H, 5.91; 6.56 (1H, d, J = 15.3), 7.13 (1H, t, J = 7.5), N, 6.27 N, 6.36 7.26-7.39 (5H, m), 7.46 (1H, brs), 7.50-7.54 (2H, m), 7.62 (2H, brd, J = 7.5), 7.76 (1H, d, J = 15.3) Ia-2 119-120 C17H17NO3 C, 72.07; H, 6.05; C, 72.06; H, 6.02; 3.81 (3H, s), 3.89 (3H, s), 6.50-6.61 (3H, m), N, 4.94 N, 5.00 7.36-7.44 (3H, m), 7.53-7.59 (2H, m), 6.69-7.77 (2H, m), 8.41 (1H, brm) Ia-3 117-118 C16H15NO2 C, 75.87; H, 5.97; C, 75.97; H, 5.93; 3.82 (3H, s), 6.55 (1H, d, J = 15.6), 6.69 N, 5.53 N, 5.49 (1H, m), 7.06 (1H, m), 7.24 (1H, t, J = 8.0), 7.36-7.55 (8H, m), 7.76 (1H, d, J = 15.6) Ia-4 154-156 C16H15NO2 C, 75.87; H, 5.97; C, 76.01; H, 6.02; 3.80 (3H, s), 6.54 (1H, d, J = 15.6), 6.88 N, 5.53 N, 5.59 (2H, d, J = 9.2), 7.35-7.55 (8H, m), 7.74 (1H, d, J = 15.6) Ia-5 195-196 C13H11N3O C, 69.32; H, 4.92; C, 69.34; H, 5.08; 6.55 (1H, d, J = 15.6), 7.41-7.44 (3H, m), N, 18.65 N, 18.56 7.55-7.59 (2H, m), 7.82 (1H, d, J = 15.6), 8.12 (1H, brs), 8.30 (1H, dd, J = 5.7, 0.9), 8.66 (1H, d, J = 5.6), 8.89 (1H, d, J = 0.9) Ia-6 143-144 C14H12N2O C, 74.98; H, 5.39; C, 74.81; H, 5.33; 6.56 (1H, d, J = 15.6), 7.07 (1H, dd, J = 7.2, N, 12.49 N, 12.72 4.8), 7.38-7.42 (3H, m), 7.54-7.57 (2H, m), 7.76 (1H, ddd, J = 8.4, 7.2, 1.8), 7.79 (1H, d, J = 15.6), 8.30 (1H, m), 8.37 (1H, d, J = 8.4), 8.40 (1H, brs) Ia-7   179-180.5 C14H12N2O C, 74.98; H, 5.09; C, 74.87; H, 5.54; 6.60 (1H, d, J = 15.3), 7.29 (1H, dd, N, 12.49 N, 12.37 J = 8.1, 4.5), 7.38-7.40 (3H, m), 7.51-7.55 (2H, m), 7.79 (1H, d, J = 15.6), 7.83 (1H, brs), 8.32 (1H, dd, J = 8.1, 1.8), 8.37 (1H, d, J = 4.5), 8.64 (1H, d, J = 1.8) Ia-9 177-178 C17H13N3O C, 74.17; H, 4.76; C, 72.51; H, 4.57; *1) 6.63 (1H, d, J = 15.4), 6.81 (1H, d, N, 15.26 N, 14.18 J = 15.4), 7.33-7.96 (8H, m), 8.12 (1H, m), 8.39 (1H, br, s), 9.99 (1H, s) Ia-10 115-116 C16H16N2O C, 76.16; H, 6.39; C, 76.35; H, 6.35; 2.35 (3H, s), 2.42 (3H, s), 6.51 (1H, d, N, 11.10 N, 11.16 J = 15.6), 6.76 (1H, s), 7.38-7.42 (3H, m), 7.52-7.56 (2H, m), 7.75 (1H, d, J = 15.6), 8.00 (1H, s), 8.14 (1H, brs) *1) NMR solvent CDCl3 + CD3OD *2) NMR solvent DMSO-d6 *3) commercially available

TABLE 15 Ia-16 136-138 C15H14N2O C, 75.61; H, 5.92; C, 75.69; H, 5.87; 2.38 (s, 3H), 6.52 (d, 1H, J = 15.6), 7.03-7.08 (m, 1H), 7.20 N, 11.76 N, 11.71 (d, 2H, J = 8.1), 7.44 (d, 2H, J = 8.1), 7.71-7.77 (m, 1H), 7.76 (d, 1H, J = 15.6), 8.29-8.31 (m, 1H), 8.37 (h, 1H, J = 8.4), 8.45 (br, 1H) Ia-17 117.5-119   C15H14N2O C, 75.61; H, 5.92; C, 75.32; H, 5.84; 2.38 (s, 3H), 6.56 (d, 1H, J = 15.6), 7.04-7.09 (m, 1H), N, 11.76 N, 11.77 7.19-7.22 (m, 1H), 7.22-7.35 (m, 3H), 7.72-7.77 (m, 1H), 7.76 (dm 1H, J = 15.6), 8.30-8.33 (m, 1H), 8.38 (d, 1H, J = 8.1), 8.57 (br, 1H) Ia-18 145-146 C15H14N2O C, 75.61; H, 5.92; C, 75.57; H, 5.84; 2.46 (s, 3H), 6.48 (d, 1H, J = 15.3), 7.04-7.09 (m, 1H), N, 11.76 N, 11.72 7.19-7.29 (m, 3H), 7.53-7.56 (m, 1H), 7.72-7.78 (m, 1H), 8.09 (d, 1H, J = 15.3), 8.30-8.32 (m, 1H), 8.38 (d, 1H, J = 8.4), 8.56 (br, 1H) Ia-23 C16H16N2O C, 76.16; H, 6.39; *1) 2.29 (6H, s), 6.53 (1H, d, J = 15.3), 7.04-7.08 (1H, m), N, 11.10 7.15 (1H, m, J = 7.8), 7.26-7.30 (2H, m), 7.74 (1H, d, J = 15.3), 7.72-7.78 (1H, m), 8.31-8.33 (1H, m), 8.39 (1H, d, J = 8.4). 8.71 (1H, br) Ia-27 186-188 C14H13N3O C, 70.28; H, 5.48; 2.48 (3H, s), 6.61 (1H, d, J = 15.6), 6.94 (1H, d, J = 7.5), N, 17.56 7.26-7.37 (1H, m), 7.62-7.67 (1H, m), 7.77 (1H, d, J = 15.6), 7.81-7.85 (1H, m), 8.14 (1H, d, J = 8.4), 8.31 (1H, br), 8.62-8.64 (1H, m), 8.79 (1H, d, J = 1.5) Ia-29   142-143.5 C16H16N2O3 C, 67.59; H, 5.67; C, 67.52; H, 5.63; *1) 3.85 (3H, s), 3.88 (3H, s), 6.47-6.54 (2H, m), 6.63 (1H, N, 9.85 N, 9.77 d, J = 15.6), 7.01-7.05 (1H, m), 7.44 (1H, d, J = 8.7), 7.70-7.76 (1H, m), 7.93 (1H, d, J = 15.6), 8.29-8.31 (2H, m), 8.37 (1H, d, J = 8.7) Ia-30 199-201 C15H11N2O C, 61.15; H, 3.79; C, 61.67; H, 3.80; 6.65 (1H, d, J = 15.6), 7.06-7.13 (1H, m), 7.65 (4H, t, J = 9.6 N, 9.59; F, 19.50 N, 9.61; F, 19.37 ), 7.72-7.81 (1H, m), 7.81 (1H, d, J = 15.6), 8.29-8.35 (1H, m), 8.37 (1H, d, J = 8.1), 8.65 (1H, br) Ia-37 189.5-191.5 C13H10N3OCl C, 60.12; H, 3.88; C, 60.33; H, 3.80; *1) 6.62 (1H, d, J = 15.6), 7.08-7.12 (1H, m), 7.28-7.32 (1H, N, 16.18; Cl, 13.65 N, 16.27; Cl, 13.6 m), 7.75-7.80 (1H, m), 7.89-7.92 (1H, m), 8.08 (1H, d, J = 15.6), 8.31-8.43 (3H, m), 8.74 (1H, br)

TABLE 16 Ia-38 200.5-202.5 C14H11N2OCl C, 65.00; H, C, 65.02; H, *1) 6.57 (1H, d, J = 15.5), 7.02-7.12 (1H, m), 7.33-7.42 4.29; N, 10.83; 4.20; N, (3H, m), 7.51 (1H, m), 7.72 (1H, d, J = 15.5), 7.74-7.79 Cl, 13.70 10.93; Cl, (1H, m), 8.32-8.38 (2H, m), 8.68 (1H, br) 13.70 Ia-39   177-178.5 C14H11N2OCl C, 65.00; H, C, 65.01; H, *1) 6.54 (1H, d, J = 15.5), 7.06-7.10 (1H, m), 7.37 (2H, 4.29; N, 4.32; N, d, J = 8.4), 7.47 (2H, d, J = 8.4), 7.74 (1H, d, 10.83; Cl, 10.93; Cl, J = 15.5), 7.73-7.79 (1H, m), 8.30-8.32 (1H, m), 8.36 13.70 13.65 (1H, d, J = 8.4), 8.58 (1H, br) Ia-40 131-132 C14H10N2OCl2 C, 57.36; H, C, 57.33; H, 6.55 (1H, d, J = 15.6), 7.05-7.13 (1H, m), 7.36 (1H, 3.44; N, 9.56; 3.35; N, 9.64; dd, J = 2.1, 8.4), 7.48 (1H, d, J = 8.1), 7.62 Cl, 24.19 Cl, 24.08 (1H, d, J = 2.4), 7.68 (1H, d, J = 15.6), 7.72-7.81 (1H, m), 8.28-8.38 (2H, m), 8.46 (1H, br) Ia-42 205-206 C13H10N3OCl C, 60.12; H, C, 60.28; H, *2) 7.15 (d, 1H, J = 15.9), 7.13-7.16 (m, 1H), 7.63 3.88; N, 3.88; N, (d, 1H, J = 8.4), 7.68 (d, 1H, J = 15.9), 16.88; Cl, 16.26; Cl, 7.80-7.86 (m, 1H), 8.07 (dd, 1H, J = 2.4 and J = 13.65 13.57 8.4), 8.24 (d, 1H, J = 7.8), 8.35-8.37 (m, 1H), 8.66 (d, 1H, J = 2.4), 10.75 (s, 1H) Ia-44 147-149 C14H11N2OF C, 69.41; H, C, 69, 60; H, 6.49 (d, 1H, J = 15.5), 7.05-7.12 (m, 3H), 4.58; N, 4.56; N, 7.50-7.55 (2H, m), 7.73-7.78 (m, 2H), 8.30-8.33 11.56; F, 7.84 11.60; F, 7.90 (1H, m), 8.36 (d, 1H, J = 8.1), 8.58 (br, 1H) Ia-45 171-172 C14H11N2OF C, 69.41; H, C, 69.53; H, 6.68 (d, 1H, J = 15.4), 7.05-7.42 (m, 5H), 7.75 4.58; N, 4.55; N, (d, 1H, J = 15.4), 7.72-7.81 (m, 1H), 8.31-8.40 11.56; F, 7.84 11.65; F, 7.89 (m, 2H), 8.82 (br, 1H) Ia-48   154-154.5 C14H11N2OF C, 69.41; H, C, 69.58; H, 6.74 (d, 1H, J = 16.2), 7.05-7.21 (m, 3H), 4.58; N, 4.52; N, 7.30-7.41 (m, 1H), 7.47-7.55 (m, 1H), 7.72-7.81 11.56; F, 7.84 11.61; F, 7.97 (m, 1H), 7.87 (d, 1H, J = 16.2), 8.32-8.35 (m, 1H), 8.39 (d, 1H, J = 8.4), 8.99 (br, 1H) Ia-46 181-182 C13H10N3OF C, 64.29; H, C, 64.48; H, 6.59 (1H, d, J = 15.6), 6.99 (1H, dd, J = 4.14; N, 4.20; N, 3.0 and 8.4), 7.08-7.13 (1H, m), 7.75-7.80 (2H, m), 17.28; F, 7.81 17.18; F, 7.63 7.92-7.99 (1H, m), 8.31-8.38 (2H, m), 8.39 (1H, d, J = 2.4), 8.79 (1H, br) Ia-53 158.5-159.5 C18H20N2O3 C, 69.21; H, C, 69.29; H, *1) 1.48 (3H, t, J = 6.9), 1.48 (3H, t, J = 6.45; N, 8.97 6.37; N, 8.99 6.9), 4.12 (2H, q, J = 6.9), 4.14 (2H, q, J = 6.9), 6.41 (1H, d, J = 15.5), 6.87 (1H, d, J = 8.4), 7.03-7.12 (3H, m); 7.70 (1H, d, J = 15.5), 7.71-7.77 (1H, m), 8.29-8.32 (1H, m), 8.37 (1H, d, J = 8.4), 8.43 (1H, br)

TABLE 17 Ia-54 148.5-149.5 C16H16N2O3 C, 67.59; H, C, 67.70; H, *1) 3.87 (3H, s), 3.89 (3H, s), 6.68 (1H, d, J = 15.8), 5.67; N, 9.85 5.59; N, 9.78 6.93-6.97 (1H, m), 7.04-7.16 (3H, m), 7.72-7.78 (1H, m), 8.05 (1H, d, J = 15.8), 8.30-8.33 (1H, m), 8.38 (1H, d, J = 8.4), 8.58 (1H, br) Ia-55   157-158.5 C16H16N2O3 C, 67.59; H, C, 67.73; H, 3.92 (s, 6H), 6.45 (d, 1H, J = 15.5), 6.88 (d, 1H, J = 8.1), 5.67; N, 9.85 5.55; N, 9.90 7.03-7.08 (m, 2H), 7.12-7.15 (m, 1H), 7.71-7.77 (m, 1H), 7.72 (d, 1H, J = 15.5), 8.30-8.32 (m, 1H), 8.37 (d, 1H, J = 8.7), 8.55 (br, 1H) Ia-59 181-182 C16H16N2O3 C, 67.59; H, C, 67.64; H, *1) 3.80 (3H, s), 3.84 (3H, s), 6.72 (1H, d, J = 15.5), 5.67; N, 9.85 5.44; N, 9.88 6.85-6.94 (2H, m), 7.04-7.08 (2H, m), 7.17-7.77 (1H, m), 7.98 (1H, d, J = 15.5), 8.30-8.33 (1H, m), 8.38 (1H, d, J = 8.4), 8.59 (1H, br) Ia-60 171-173 C16H16N2O3 C, 67.59; H, C, 67.57; H, *1) 3.82 (6H, s), 6.50-6.51 (1H, m), 6.54 (1H, d, J = 15.9), 5.67; N, 9.85 5.57; N, 9.90 6.68 (2H, d, J = 2.1), 7.05-7.09 (1H, m), 7.70 (1H, d, J = 15.9), 7.72-7.78 (1H, m), 8.31-8.33 (1H, m), 8.37 (1H, d, J = 8.7), 8.62 (1H, br) Ia-61 141-143 C17H17NO3 C, 72.07; H, C, 71.85; H, 3.86 (3H, s), 3.88 (3H, s), 6.65 (1H, d, J = 15.6), 6.91- 6.05; N, 4.94 6.03; N, 5.01 7.39 (6H, m), 7.47 (1H, brs), 7.63 (1H, brd, J = 8.0) Ia-62 amorphous C17H17NO3 C, 72.07; H, C, 72.01; H, 3.93 (3H, s), 3.94 (3H, s), 6.39 (1H, d, J = 15.9), 6.90 (1H, 6.05; N, 4.94 6.18; N, 5.11 d, J = 8.7), 7.08-7.39 (8H, m), 7.80 (1H, d, J = 15.9) Ia-63 170.5-172   C17H17NO3 C, 72.07; H, C, 72.11; H, 3.80 (3H, s), 3.86 (3H, s), 6.68 (1H, d, J = 15.4), 6.83- 6.05; N, 4.94 6.08; N, 5.06 7.39 (6H, m), 7.40 (1H, brs), 7.62 (2H, brd, J = 8.0) Ia-64 141-142 C18H19NO4 C, 68.99; H, C, 69.09; H, 3.80 (3H, s), 3.85 (3H, s), 3.87 (3H, s), 6.64 (1H, d, 6.11; N, 4.47 6.02; N, 4.43 J = 15.6), 6.85-7.13 (5H, m), 7.47 (1H, brs), 7.55 (2H, brd) Ia-65 168.5-169.5 C18H19NO4 C, 68.99; H, C, 69.13; H, 3.81 (3H, s), 3.91 (6H, s), 6.41 (1H, d, J = 15.4), 6.85- 6.11; N, 4.47 6:08; H, 4.48 7.15 (5H, m), 7.52 (2H, brd, J = 8), 7.68 (1H, d, J = 15.4) Ia-69 129.5-131.5 C17H18N2O4 C, 64.94; H, 3.89 (9H, s), 6.50 (1H, d, J-5.5), 6.76 (2H, s), 7.05-7.09 5.77; N, 8.91 (1H, m), 7.70 (1H, d, J = 15.5), 7.73-7.79 (1H, m), 8.32-8.34 (1H, m), 8.38 (1H, d, J = 8.1), 8.85 (1H, br)

TABLE 18 Ia-77 179-180 C16H16N2O3 C, 67.59; H, C, 67.46; H, *1) 3.87 (6H, s), 6.57 (2H, d, J = 8.7), 7.01-7.05 (1H, m), 7.08 5.67; N, 9.85 5.66; N, 9.80 (1H, d, J = 15.9), 7.25-7.30 (1H, m), 7.70-7.76 (1H, m), 8.23 (1H, d, J = 15.9), 8.29-8.32 (1H, m), 8.41 (1H, d, J = 8.4), 8.56 (1H, br) Ia-95 180-182 C13H12N4O C, 64.99; H, C, 65.09; H, *2) 5.80 (br 2H), 6.20-6.23 (m, 1H), 7.15 (d, 1H, J = 15.9), 5.03; N, 23.32 5.05; N, 23.25 7.38-7.40 (m, 2H), 7.46-7.50 (m, 1H), 7.61 (d, 1H, d = 15.9), 7.97-7.99 (m, 1H), 8.57-8.59 (m, 1H), 8.79 (d, 1H, J = 1.8), 10.12 (s, 1H) Ia-97 249-251 C14H14N4O C, 66.13; H, *2) 2.82 (3H, d, J = 4.8), 6.53 (1H, d, J = 9.0), 6.75 (1H, d, J = 5.55; N, 22.03 15.6), 7.07-7.11 (2H, m), 7.50 (1H, d, J = 15.6), 7.61 (1H, dd, J = 2.3 and 9.0), 7.76-7.81 (1H, m), 8.21-8.25 (2H, m), 8.31-8.34 (1H, m), 10.49 (1H, s) Ia-104 157-158 C12H10N2O2 C, 67.28; H, C, 67.58; H, 6.47 (1H, d, J = 15.6), 6.48 (1H, dd, J = 3.3, 1.8), 6.62 (1H, 4.71; N, 13.08 4.77; N, 13.10 d, J = 3.3), 7.06 (1H, ddd, J = 7.2, 4.8, 0.9), 7.48 (1H, d, J = 1.8), 7.55 (1H, d, J = 15.6), 7.73 (1H, ddd, J = 8.1, 7.2, 1.8), 8.30 (1H, m), 8.35 (1H, d, J = 8.1), 8.48 (1H, brs) Ia-105 140-141 C12H10N2OS C, 62.59; H, C, 62.78; H, 6.40 (1H, d, J = 15.3), 7.06 (1H, dd, J = 5.1, 3.6), 7.08 (1H, 4.38; N, 12.16; 4.42; N, 12.07; ddd, J = 8.0, 4.8, 0.9), 7.26 (1H, d, J = 3.6), 7.36 (1H, d, J = 5.1), S, 13.92 S, 13.99 7.75 (1H, ddd, J = 8.7, 8.0, 2.1), 7.90 (1H, d, J = 15.3), 8.33 (1H, m), 8.38 (1H, d, J = 8.7), 9.02 (1H, brs) Ia-112 208-209 C13H11N3O C, 69.32; H, C, 69.48; H, *1) 6.85 (1H, d, J = 15.6), 7.10 (1H, ddd, J = 6.3, 5.1, 1.2), 4.92; N, 18.66 4.87; N, 18.73 7.40 (1H, dd, J = 8.1, 5.1), 7.75 (1H, d, J = 15.6), 7.78 (1H, ddd, J = 8.4, 6.3, 2.1), 7.94 (1H, ddd, J = 8.1, 2.4, 1.2), 8.29 (1H, m), 8.35 (1H, d, J = 8.4), 8.56 (1H, dd, J = 5.1, 1.2), 8.77 (1H, d, J = 2.4) Ia-113 178-179 C13H11N3O C, 69.32; H, C, 69.32; H, 7.06 (1H, ddd, J = 8.4, 5.1, 0.9), 7.16 (1H, d, J = 15.3), 7.28 (1H, 4.92; N, 18.6 4.97; N, 18.71 ddd, J = 7.5, 4.8, 1.2), 7.41 (1H, d, J = 7.5), 7.73 (1H, dt, J = 7.5, 1.8), 7.76 (1H, td, J = 8.4, 1.8), 7.77 (1H, d, J = 15.3), 8.33 (1H, m), 8.36 (1H, d, J = 8.4), 8.65 (1H, m)

TABLE 19 Ia-118 150.5-152   C12H10NO2 C, 67.28; H, C, 67.23; H, 6.30 (d, 1H, J = 15.6), 6.56-6.57 (m, 1H), 7.05-7.09 (m, 1H), 4.70; N, 13.08 4.73; N, 13.08 7.43-7.45 (m, 1H), 7.66-7.78 (m, 3H), 8.30-8.33 (m, 1H), 8.37 (d, 1H, J = 7.2), 8.77 (br, 1H) Ia-119 1555.5-156.5  C12H10N2OS C, 62.59; H, C, 62.64; H, 6.40 (1H, d, J = 15.3), 7.06 (1H, ddd, J = 7.5, 4.8, 1.2), 7.27 4.38; N, 12.16; 4.41; N, 12.10; (1H, m), 7.35 (1H, m), 7.51 (1H, dd, J = 2.7, 0.9), 7.75 (1H, S, 13.92 S, 13.94 ddd, J = 8.4, 7.5, 1.8), 7.77 (1H, d, J = 15.3), 8.30 (1H, m), 8.36 (1H, d, J = 8.4), 8.80 (1H, brs) Ia-120 179-181 C13H11N3O C, 69.32; H, C, 69.35; H, 6.76 (d, 1H, J = 15.6), 7.09-7.13 (m, 1H), 7.36-7.38 (m, 2H), 4.92; N, 18.65 4.88; N, 18.67 7.72 (d, 1H, J = 15.6), 7.75-7.81 (m, 1H), 8.32-8.38 (m, 2H), 8.66-8.68 (m, 2H), 8.90 (br, 1H) Ia-131 212-215 C17H14N2O2 C, 73.37; H, C, 73.58; H, 4.98 (2H, s), 5.87 (1H, d, J = 15.3), 6.84 (1H, d, J = 8.1), 5.07; N, 10.07 4.83; N, 10.14 6.87-6.97 (1H, m), 7.00-7.23 (3H, m), 7.48 (1H, d, J = 15.3), 7.70-7.79 (1H, m), 8.26-8.36 (2H, m), 8.39 (1H, br) Ia-144 140-141 C16H15NO2 C, 75.87; H, C, 75.88; H, 3.84 (3H, s), 6.43 (1H, d, J = 15.6), 6.94 (2H, d, J = 8.8), 5.97; N, 5.53 5.90; N, 5.63 7.12 (1H, m), 7.34 (2H, m), 7.45 (1H, brs), 7.47 (2H, d, J = 8.8), 7.61 (2H, brd, J = 8), 6.71 (1H, d, J = 15.6) Ia-145 104-105 C16H15NO2 C, 75.87; H, C, 75.83; H, 3.84 (3H, s), 6.93 (1H, m), 7.06 (1H, m), 7.14 (2H, m), 5.97; N, 5.53 6.08; N, 5.61 7.28-7.38 (4H, m), 7.62 (2H, brd), 7.73 (1H, d, J = 15.6) Ia-146 164-166 C16H15NO2 C, 75.87; H, C, 76.10; H, 3.89 (3H, s), 6.70 (1H, d, J = 15.6), 6.90-6.98 (2H, m), 5.97; N, 5.53 5.93; N, 5.53 7.08-7.15 (1H, m), 7.30-7.50 (5H, m), 7.63 (2H, brd, J = 8.0), 8.00 (1H, d, J = 15.6) Ia-150 207-209 C14H13N3O2 C, 65.87; H, C, 65.92; H, 2) 3.91 (3H, s), 6.94 (1H, d, J = 8.7), 7.48 (1H, d, J = 15.8), 5.17; N, 16.46 5.27; N, 16.42 7.10-7.14 (1H, m), 7.64 (1H, d, J = 15.8), 7.78-7.84 (1H, m), 7.94 (1H, dd, J = 2.4 and 8.7), 8.24 (1H, d, J = 8.4), 8.33-8.36 (1H, m), 8.42 (1H, d, J = 2.4), 10.65 (1H, a) Ia-151 185-186 C17H17NO30.2H2O C, 72.07; H, C, 71.16; H, 3.80 (3H, s), 3.84 (3H, s), 6.40 (1H, d, J = 15.6), 6.86-6.92 6.05; N, 4.94 6.11; N, 4.88 (4H, m), 6.45-7.53 (4H, m), 7.69 (1H, d, J = 15.6) Ia-152 119.5-121   C15H14N2O2 C, 70.85; H, C, 70.91; H, 3.83 (s, 3H), 6.57 (d, 1H, J = 15.4), 6.91-6.96 (m, 1H), 7.04- 5.55; N, 11.02 5.46; N, 11.01 7.15 (m, 3H), 7.27-7.35 (m, 1H), 7.72-7.79 (m, 2H), 8.31-8.33 (m, 1H), 8.34 (d, 1H, J = 8.4), 8.75 (br, 1H)

TABLE 20 Ia-153 130-131 C15H14N2O2 C, 70.85; H, C, 70.89; H, 3.85 (3H, s), 6.43 (1H, d, J = 15.3), 6.92 (2H, d, J = 8.7), 7.05 5.55; N, 11.02 5.26; N, 11.02 (1H, ddd, J = 7.2, 5.1, 1.2), 7.49 (2H, d, J = 8.7), 7.74 (1H, d, J = 15.3), 7.74 (1H, ddd, J = 8.4, 7.2, 2.1), 8.30 (1H, m), 8.36 (1H, d, J = 8.4), 8.36 (1H, brs) Ia-156   137-138.5 C15H14N2O2 C, 70.85; H, C, 70.77; H, *1) 3.89 (3H, s), 6.74 (1H, d, J = 15.6), 6.92-7.07 (3H, m), 7.33- 5.55; N, 11.02 5.44; N, 11.06 7.38 (1H, m), 7.49-7.52 (1H, m), 7.71-7.77 (1H, m), 8.02 (1H, d, J = 15.6), 8.30-8.40 (1H, m), 8.39 (1H, d, J = 8.2), 8.55 (1H, br) Ia-161   199-200.5 C15H12N2O3 C, 67.16; H, C, 67.27; H, 6.02 (s, 2H), 6.39 (d, 1H, J = 15.5), 6.82 (d, 1H, J = 8.4), 4.51; N, 10.44 4.46; N, 10.45 7.01-1.08 (m, 3H), 7.69 (d, 1H, J = 15.5), 7.71-7.77 (m, 1H), 8.30-8.38 (m, 2H), 8.53 (br, 1H) Ia-162 177-178 C17H15NO4 C, 68.68; H, C, 68.54; H, 3.80 (3H, s), 6.00 (2H, s), 6.35 (1H, d, J = 15.6), 6.80-7.02 5.09; N, 4.71 5, 06; N, 4.71 (5H, m), 7.25 (1H, brs), 7.52 (2H, brd, J = 7.8), 7.65 (1H, d, J = 15.6) Ia-177 272.5-274   C14H10N4OS C, 59.56; H, C, 59.26; H, *2) 7.13-7.17 (1H, m), 7.28 (1H, d, J = 15.8), 7.81-7.87 (1H, m), (dec) 3.57; N, 19.84; 3.56; N, 19.65; 7.89 (1H, d, J = 15.8), 7.94-7.97 (1H, m), 8.19 (1H, d, J = 9.6), S, 11.36 S, 11.32 8.27 (1H, d, J = 8.4), 8.36-8.39 (2H, m), 10.79 (1H, s) Ia-203 295-297 C10H8N4OS C, 51.71; H, C, 51.69; H, *2) 7.05 (1H, d, J = 15.9), 7.51 (1H, dd, J = 4.8, 7.8), 7.83 (dec) 3.47; N, 24.12; 3.47; N, 24.06; (1H, d, J = 15.9), 8.07 (1H, d, J = 7.8), 8.63 (1H, d, J = 4.8), 8.85 (1H, S, 13.81 S, 13.68 s), 9.21 (1H, s), 12.88 (1H, br) Ia-204 252-254 C11H9N3OS C, 57.13; H, C, 57.10; H, *2) 7.02 (1H, d, J = 15.9), 7.27 (1H, d, J = 3.6), 7.50 (1H, dd, J = 3.92; N, 18.17; 3.92; N, 18.20; 4.8, 8.1), 7.53 (1H, d, J = 3.6), 7.77 (1H, d, J = 15.9), 8.01-8.08 S, 13.86 S, 13.76 (1H, m), 8.61 (1H, dd, J = 1.8, 4.8), 8.83 (1H, d, J = 1.8), 12.42 (1H, br) Ib-1 162-164 C13H11NO C, 79.16; H, C, 78.98; H, 7.12-7.20 (1H, m), 7.34-7.67 (7H, m), 7.85-7.90 (3H, m) 5.62; N, 7.10 5.62; N, 7.13 Ib-2 69-70 C15H15NO2 C, 74.67; H, C, 74.60; H, 1.64 (t, 3H, J = 7.1), 4.29 (q, 2H, J = 7.1), 7.01 (d, 1H, J = 8.1), 6.27; N, 5.80 6.18; N, 5.93 7.10-7.15 (m, 2H), 7.34-7.39 (m, 2 H), 7.44-7.50 (m, 1H), 7.67-7.70 (m, 2H), 8.31 (dd, 1H, J = 2.0 and 7.7), 10.13 (1H, br)

TABLE 21 Ib-3 161.5-162.5 C15H11NO2 C, 75.94; H, C, 76.04; H, 7.18 (1H, t, J = 7.5), 7.33-7.74 (8H, m), 8.34 (1H, brs) 4.67; N, 5.90 4.59; N, 6.04 Ib-4 142.5-143.5 C15H15NO C, 79.97; H, C, 79.73; H, 2.34 (3H, s), 2.50 (3H, s), 7.17 (2H, d, J = 8.4), 7.25-7.27 6.71; N, 6.22 6.72; N, 6.25 (2H, m), 7.33-7.39 (1H, m), 7.41 (1H, br), 7.46-7.75 (3H, m) Ib-5 oil C15H15NO2 C, 74.67; H, C, 74.32; H, 2.34 (3H, s), 4.05 (3H, s), 7.03 (1H, d, J = 8.4), 7.11-7.16 6.27; N, 5.80 6.26; H, 5.77 (1H, m), 7.16 (2H, d, J = 8.1), 7.46-7.52 (1H, m), 7.56 (2H, d, J = 8.1), 8.29 (1H, dd, J = 1.8 and 7.8), 9.73 (1H, br) Ib-6 132-133 C14H12ClNO C, 68.44; H, C, 68.25; N, 2.35 (3H, s), 7.18 (2H, d, J = 8.4), 7.36-7.47 (3H, m), 7.53 4.92; N, 5.70; 4.96; N, 5.78; (2H, d, J = 8.4), 7.74-7.79 (1H, m), 7.82 (1H, br) Cl, 14.43 Cl, 14.40 Ib-7 107-109 C15H15NO C, 79.97; H, C, 79.71; H, 2.34 (3H, s), 2.43 (3H, s), 7.17 (2H, d, J = 8.4), 7.35-7.37 6.71; N, 6.22 6.72; N, 6.26 (2H, m), 7.52 (2H, d, J = 8.4), 7.62-7.65 (1H, m), 7.68 (1H, s), 7.74 (1H, br) Ib-8 127-129 C15H15NO2 C, 74.67; H, C, 74.59; H, 2.34 (3H, s), 3.86 (3H, s), 7.05-7.10 (1H, m), 7.17 (2H, d, J = 6.27; N, 5.80 6.31; N, 5.86 8.4), 7.36-7.38 (2H, m), 7.43-7.44 (1H, m), 7.51 (2H, d, J = 8.4), 7.77 (1H, br) Ib-9   122-124.5 C14H12ClNO C, 68.44; H, C, 68.42; H, 2.35 (3H, s), 7.19 (2H, d, J = 8.1), 7.40-7.45 (1H, m), 4.92; N, 5.70; 4.95; N, 5.77; 7.50-7.54 (3H, m), 7.72-7.75 (2H, m), 7.85-7.86 (1H, m) Cl, 14.43 Cl, 14.44 Ib-10   198-199.5 C18H15NO C, 89.73; H, C, 89.82; H, *2) 2.30 (3H, s), 7.18 (2H, d, J = 8.7), 7.58-7.63 (3H, m), 5.79; N, 5.36 5.70; N, 5.46 7.68-7.75 (3H, m), 8.00-8.08 (2H, m), 8.16-8.19 (1H, m), 10.48 (1H, s) Ib-11 *3 Ib-12 173-175 C15H13NO2 C, 75.30; H, 2.35 (s, 3H), 7.18-7.20 (m, 3H), 7.53 (d, 2H, J = 8.4), 7.86 5.48; N, 5.85 (br, 1H), 7.96-8.03 (m, 3H), 10.10 (s, 1H) Ib-13 202-204 C16H15NO3 C, 74.67; H, C, 74.59; H, *2) 2.29 (s, 3H), 3.90 (s, 3H), 7.17 (d, 2H, J = 8.6), 7.66 (d, 6.29; N, 5.80 6.31; N, 5.86 2H, J = 8.6), 8.07-8.08 (m, 4H), 10.35 (s, 1H) Ib-14 312-314 C15H13NO3 C, 70.58; H, C, 10.81; H, 2.28 (s, 3H), 7.16 (d, 2H, J = 8.4), 7.70 (d, 2H, J = 8.4), 5.13; N, 5.49 5.22; N, 5.70 8.05-8.06 (m, 4H), 10.45 (s, 1H)

TABLE 22 Ib-15 206.5-208.5 C19H19NO3 C, 73.77; H, C, 73.94; H, *2) 1.28 (t, 3H, J = 7.1), 2.28 (s, 3H), 4.22 (q, 2H, J = 7.1), 6.19; N, 4.53 6.09; N, 4.82 6.78 (d, 1H, J = 16.2), 7.16 (d, 2H, J = 8.4), 7.66 (d, 2H, J = 8.4), 7.71 (d, 1H, J = 16.2), 7.88 (d, 2H, J = 8.4), 7.98 (d, 2H, J = 8.4). 10.23 (s, 1H) Ib-16 300-302 C17H15NO3 C, 72.58: H, C, 72.59; H, *2) 2.28 (3H, s), 6.67 (1H, d, J = 16.2), 7.16 (2H, d, J = 8.7), (dec) 5.37; 5.98 5.43; N, 5.35 7.66 (1H, d, J = 16.2), 7.66 (2H, d, J = 8.7), 7.85 (2H, d, J = 8.4), 7.98 (2H, d, J = 8.4), 10.22 (1H, s) Ib-17 215-217 C14H12NOCl C, 68.43; H, C, 68.53; H, *2) 2.28 (3H, s), 7.16 (2H, d, J = 8.9), 7.60 (2H, d, J = 8.9), 4.92; N, 5.70 5.01; N, 5.84 7.65 (2H, d, J = 8.9), 7.98 (2H, d, J = 8.9) Ib-18 155-157 C15H15NO2 C, 74.67; H, C, 74.74; H, 2.34 (s, 3H), 3.87 (s, 3H), 6.97 (d, 2H, J = 8.8), 7.16 (d, 2H, , 6.72; N, 5.80 6.19; N, 5.88 J = 8.2), 7.51 (d, 2H, J = 8.2), 7.70 (br, 1H), 7.83 (d, 2H, J = 8.8) Ib-19 174-175 C16H17NO2 C, 75.27; H, C, 75.32; H, 1.45 (3H, t, J = 7.2), 2.33 (3H, s), 4.09 (2H, q, J = 7.2), 6.95 6.71; N, 5.49 6.63; N, 5.56 (2H, d, J = 9.0), 7.16 (2H, d, J = 8.6), 7.50 (2H, d, J = 8.6), 7.69 ( 1H, br), 7.82 (2H, d, J = 9.0) Ib-20 192-194 C18H15NO C, 82.73; H, C, 82.72; H, *2) 3.33 (3H, s), 7.18 (2H, d, J = 8.4), 7.12-7.65 (2H, m), 7.71 5.79; N, 5.36 5.82; N, 5.45 (2H, d, J = 8.4), 8.00-8.10 (4H, m), 8.57 (1H, s), 10.35 (1H, s) Ib-21 *3 Ib-22 150-155 C19H23NO C, 81.10; H, C, 80.85; H, 1.25 (3H, d, J = 6.6), 1.28 (3H, d, J = 6.6), 2.81-3.07 (1H, m), 8.24; N, 4.98 8.31; N, 5.19 7.22 (2H, d, J = 8.9), 7.33 (2H, d, J = 8.9), 7.55 (2H, d, J = 8.9), 7.79 (2H, d, J = 8.9) Ib-23 *3 Ib-24 158-159 C14H13NO2 C, 73.99; H, C, 74.02; H, 3.82 (3H, s), 6.91 (2H, d, J = 9.2), 7.43-7.6 (5H, m), 7.76 5.77; N, 6.16 5.83; N, 6.25 (1H, brs), 7.84-7.89 (2H, m) Ib-25 *3 Ib-26 215-216 C14H12NOCl C, 68.43; H, C, 68.52; H, *2) 2.39 (3H, s), 7.34 (2H, d, J = 8.6), 7.40 (2H, d, J = 9.2), 4.92; N, 5.70 4.89; N, 5.86 7.82 (2H, d, J = 9.2), 7.87 (2H, d, J = 8.6) Ib-27 oil C14H13NO 2.26 (3H, s), 2.28 (3H, s), 3.46 (3H, s), 6.89-7.05 (6H, m), 7.19 (2H, d, J = 8.2),

TABLE 23 Ib-28 213-214 C13H9NOC12 C, 58.67; H, C, 58.45; H, *2) 7.42 (2H, d, J = 9.2), 7.62 (2H, d, J = 8.6), 7.81 (2H, d, J = 9.2), 3.41; N, 5.26 3.49; N, 5.38 7.98 (2H, d, J = 8.6) Ib-29 245-247 C20H17N1O1 C, 83.59; H, C, 83.70; H, 2.35 (3H, s), 7.39-7.52 (3H, m), 7.55 (2H, d, J = 8.4), 7.55 (2H, d, 5.96N, 4.87 5.96N, 4.87 J = 8.4), 7.57-7.66 (2H, m), 7.70 (2H, d, J = 8.4), 7.96 (2H, d, J = 8.4) Ib-30 257-258 C20H17N1O2 C, 79.19; H, C, 79.12; H, *2) 3.75 (3H, s), 6.93 (2H, d, J = 9.2), 7.42-7.55 (3H, m), 7.70 (2H, 5.65 5.57 d, J = 9.2), 7.76 (2H, m), 7.83 (2H, d, J = 8.4), 8.05 (2H, d, J = N, 4.62 N, 4.77 8.4), 10.17 (1H, s) Ib-31 256-258 C18H1NO5 C, 66.46; H, C, 66.10; H, *2) 3.77 (3H, s), 3.89 (3H, s), 6.93 (1H, s), 6.99 (2H, d, J = 8.9), (dec) 4.65; N, 4.31 4.75; N, 4.51 7.45 (1H, d, J = 3.0), 7.53 (1H, dd, J = 3.0, 9.2), 7.70 (2H, d, J = 8.9), 7.80 (1H, d, J = 9.2), 10.62 (1H, s) Ib-35 162-163 C18H14N2O C, 78.81; H, C, 78.66; H, 7.09 (1H, ddd, J = 7.2, 5.1, 1.2), 7.38-7.76 (7H, m), 7.77 (1H, 5.14; N, 10.21 5.08; N, 10.18 ddd, J = 8.4, 7.2, 2.1), 8.02 (2H, d, J = 8.1), 8.32 (1H, brd), 8.43 (1H, d, J = 8.4), 8.71 (1H, brs) Ib-73 118-119 C11H9N3O C, 66.32; H, C, 66.37; H, 7.08 (1H, ddd, J = 7.5, 4.8, 1.2), 7.50 (1H, ddd, J = 7.8, 4.8, 1.2), 4.55; N, 21.09 4.48; S, 21.02 7.77 (1H, ddd, J = 8.1, 7.5, 1.8), 7.91 (1H, td, J = 7.8, 1.8), 8.30 (1H, m), 8.36 (1H, m), 8.43 (1H, d, J = 8.1)), 8.64 (1H, m) Ib-77 138-140 C11H9N3O C, 66.32; H, C, 66.49; H, 7.11 (1H, ddd, J = 7.2, 4.8, 1.2), 7.46 (1H, ddd, J = 7.8, 4.8, 0.6), 4.55; N, 21.09 4.47; N, 20.79 7.79 (1H, ddd, J = 8.7, 7.2, 1.8), 8.25 (1H, ddd, J = 7.8, 2.4, 1.2), 8.30 (1H, m), 8.38 (1H, d, J = 8.7), 8.81 (1H, dd, J = 4.8, 1.2), 9.18 (1H, brd) Ib-80 141-142 C11H9N3O C, 66.32; H, C, 66.46; H, 7.11 (1H, ddd, J = 7.5, 4.8, 0.8), 7.80 (1H, ddd, J = 8.1, 7.5, 2.1), 4.55; N, 21.09 4.47; N, 21.15 7.76 and 8.82 (4H, AB, J = 6.0), 8.27 (1H, m), 8.37 (1H, d, J = 8.1), 8.80 (1H, brs) Ib-97 98-99 C15H13N3O0.25N2O C, 71.70; H, C, 70.43; H, 4.12 (3H, s), 7.08 (1H, dd, J = 7.0, 5.4), 7.13 (1H, s), 7.18 (1H, 5.21; N, 16.72 5.32; N, 16.43 m), 7.37 (1H, m), 7.42 (1H, d, J = 7.8), 7.69 (1H, d, J = 8.1), 7.78 (1H, ddd, J = 8.4, 7.0, 1.8), 8.33 (1H, m), 8.34 (1H, d, J = 8.1)

TABLE 24 Ib-102 140-141 C14H10N2O2 C, 70.58; H, C, 70.59; H, 7.10 (1H, ddd, J = 7.8, 5.1, 0.6), 7.33 (1H, m), 4.23; N, 11.76 4.21; N, 11.72 7.47 (1H, m), 7.56 (1H, d, J = 8.4), 7.63 (1H, s), 7.71 (1H, dd, J = 8.4, 1.2), 7.77 (1H, dt, J = 7.8, 2.1), 8.36 (1H, m), 8.38 (1H, d, J = 7.8), 9.02 (1H, brs) Ib-105 200-202 C14H11N3O C, 70.87; H, C, 70.83; H, 7.09 (1H, dd, J = 7.8, 4.8), 7.16 (1H, s), 7.16 4.67; N, 17.71 4.64; N, 17.62 (1H, m), 7.33 (1H, m), 7.45 (1H, d, J = 8.4), 7.67 (1H, d, J = 8.1), 7.75 (1H, ddd, J = 8.1, 7.8, 1.8), 8.36 (1H, m), 8.40 (1H, d, J = 8.1), 8.90 (1H, brs), 9.71 (1H, brs) Ib-122 129-131 C10H8N2OS0.1H2O C, 58.80; H, C, 58.29; H, 7.08 (1H, dd, J = 7.5, 5.1), 7.14 (1H, dd, 3.95; N, 13.72; 4.01; N, 13.60; J = 5.1, 3.9), 7.59 (1H, dd, J = 5.1, 1.2), S, 15.70 S, 15.56 7.69 (1H, dd, J = 3.9, 1.2), 7.76 (1H, ddd, J = 8.4, 7.5, 2.1), 8.30 (1H, m), 8.33 (1H, d, J = 8.4) Ib-124 106-107 C10H8N2OS C, 58.80; H, C, 58.93; H, 7.09 (1H, dd, J = 8.4, 5.7), 7.41 (1H, dd, 3.95; N, 13.72; 3.90; N, 13.62; J = 5.1, 3.0), 7.55 (1H, dd, J = 5.1, 1.5), S, 15.70 S, 15.65 7.70 (1H, td, J = 8.4, 2.0), 8.07 (1H, J = 3.0, 1.5), 8.30 (1H, m), 8.37 (1H, d, J = 8.4) Ib-131 258-260 C13H9N3O2S C, 57.55; H, 3.34; C, 57.56; H, 3.40; *2) 6.76 (1H, dd, J = 1.8, 3.6), 7.26 (1H, d, N, 15.49; S, N, 15.47; S, J = 3.6), 7.53-7.64 (2H, m), 7.65-7.74 (1H, m), 11.82 11.59 7.98 (1H, d, J = 1.8), 8.11-8.20 (2H, m), 13.24 (1H, br) Ib-133 189-191 C13H9N3O3 C, 61.18; H, 3.55; C, 61.01; H, 3.47; *2) 6.80 (1H, dd, J = 1.8, 3.6), 7.30 (1H, d, N, 16.46 H, 16.39 J = 3.6), 7.52-7.62 (2H, m), 7.63-7.72 (1H, m), 7.98-8.09 (3H, m), 12.18 (1H, br) Ib-137 126-127 C15H11N3O1 C, 72.28; H, 4.45N, C, 72.37; H, 7.57 (2H, d, J = 7.4), 7.60-7.89 (4H, m), 16.86 4.38N, 16.17 8.01 (2H, dd, J = 1.6, 8.1), 8.12 (1H, m), 8.76 (1H, br. s), 10.01 (1H, s) Ib-144 226-228 C15H10Cl1N3O1 C, 63.50; H, 3.55 C, 63.51; H, 3.76 7.53 (2H, d, J = 8.8), 7.66-7.88 (3H, m), 7.95 Cl, 12.49; N, Cl, 12.51; N, (2H, d, J = 8.8), 8.12 14.81 14.60 (1H, m), 8.71 (1H, br. s), 9.97 (1H, s) Ic-1 126-127 C16H15NO2 C, 75.87; H, C, 76.00; H, 3.84 (3H, s), 6.13 (1H, d, J = 12.3), 5.97; N, 5.53 5.89; N, 5.53 6.90-7.47 (10H, m) Ic-5 131.5-132.5 C16H17NO2 C, 75.27; H, 6.71; C, 75.21; H, 6.74; 2.63 (2H, t, J = 7.6), 3.05 (2H, t, J = N, 5.49 N, 5.53 7.6), 3.78 (3H, s), 6.81-6.86 (2H, m), 6.95 (1H, brs), 7.21-7.34 (7H, m) Id-1 159-161 C16H14N2O C, 76.78; H, 5.64; C, 76.86; H, 5.68; *1) 6.13 (1H, d, J = 14.7), 6.91-6.94 (2H, m), N, 11.19 N, 11.23 7.03-7.07 (1H, m), 7.32-7.39 (3H, m), 7.46-7.60 (3H, m), 7.70-7.76 (1H, m), 8.26 (1H, br), 8.28-8.31 (1H, m), 8.34 (1H, d, J = 8.7)

Experiment 1

Activity to Enhance the Expression of Human apoAI

The promoter region of the gene encoding human apoAI was isolated, and ligated upstream the structure gene of firefly luciferase to construct a reporter plasmid. The reporter plasmid and a marker plasmid conferring the neomycin resistance were co-infected to cell lines derived from human hepatoma, HepG2 cells, and the cell lines were incubated in a selection medium comprising DMEM medium containing 10% fetal calf serum supplemented with G418 (Final concentration: 0.7 mg/mL, Gibco) to give established strains that stably expressed the reporter molecule. The strains were seeded to a 96-well culture plates at a density of 50,000 cells per well, and incubated for 48 hours at 37° C. under an atmosphere of 5% carbon dioxide. Then, a solution of the compounds according to the invention in DMSO was added to the wells at final concentrations of 0 to 10 μg/mL. After further incubation for 24 hours, the cells were added with a luciferase assay reagent (Piccagene LT 7.5 registered trade mark, Toyo Ink, KK), and the luciferase activity was determined using a luminometer (MicroBeta™ TRILUX, 1 sec/well, Wallac). The concentration of the compounds, which intensified the luciferase activity twice compared to that of control (DMSO without any compound of the invention added) was set as the minimal effective dose (MED). The results are shown in Table 25.

TABLE 25 MED (μg/ml) Ia-1 0.13 Ia-3 0.49 Ia-4 0.54 Ia-6 0.34 Ia-16 0.21 Ia-17 0.5 Ia-30 0.14 Ia-39 0.1 Ia-42 0.8 Ia-44 0.18 Ia-45 0.54 Ia-46 0.17 Ia-61 0.31 Ia-64 0.13 Ia-95 1.2 Ia-105 0.68 Ia-144 0.08 Ia-145 0.44 Ia-152 0.22 Ia-153 0.19 Ia-161 0.14 Ib-4 0.31 Ib-6 0.71 Ib-7 0.39 Ib-8 0.46 Ib-9 1.53 Ib-11 0.28 Ib-17 0.30 Ib-18 0.22 Ib-19 0.25 Ib-20 0.81 Ib-25 0.71 Ib-26 0.33 Ib-28 0.32 Ib-35 0.21 Ib-73 1.2 Ib-105 0.81 Ib-131 0.66 Ib-137 0.72 Ib-144 0.91 Id-1 0.5

Table 25 shows that the compounds according to the invention can promote the function of the gene encoding human apoAI, thereby enhancing the expression of apoAI.

Formulation 1 Tablets compound (Ia-1) 15 mg starch 15 mg lactose 15 mg crystalline cellulose 19 mg polyvinyl alcohol 3 mg distilled water 30 mL calcium stearate 3 mg

The ingredients other than calcium stearate were mixed uniformly, and the mixture was powdered, granulated, and dried to give granules having a suitable size. Then, the calcium stearate was added and the mixture was compressed to give a tablet formulation.

Formulation 2 Capsules compound (Ia-7) 10 mg magnesium stearate 10 mg lactose 80 mg

The ingredients were homogeneously mixed to give powders or fine particles, which were formed into a powder formulation. This was filled in capsules to give a capsule formulation.

Formulation 3 Granules compound (Ia-1) 30 g lactose 265 g magnesium stearate 5 g

The ingredients were mixed thoroughly, and the mixture was compressed, powdered, granulated and sieved to give a granule formulation.

INDUSTRIAL APPLICABILITY

As is apparent from the experiment as described above, the compounds according to the invention have an activity for enhancing the expression of apoAI. Thus, the compounds according to the invention are useful as pharmaceutical compositions for preventing and/or treating dyslipidemia or arteriosclerotic diseases, and in a method and use therefor. 

1. A method of enhancing the expression of apoAI, which comprises administering a therapeutically effective amount of a compound of formula (I):

in which ring A is Ar² or a group of

Ar¹ and Ar² are independently a monocyclic or bicyclic aromatic carbocyclic group that may be optionally substituted, or a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted; ring B is a monocyclic non-aromatic carbocyclic group that may be optionally substituted, or a monocyclic non-aromatic heterocyclic group that may be optionally substituted; R is a hydrogen or a lower alkyl that may be optionally substituted; Z is oxygen or sulfur; Y¹ and Y² are independently a hydrogen, a halogen, a lower alkyl that may be optionally substituted, a carboxy, a lower alkoxycarbonyl that may be optionally substituted, a cyano, a phenyl that may be optionally substituted, or a monocyclic aromatic heterocyclic group that may be optionally substituted, and two Y's or more and two Y²S or more each may be different among them; n is an integer of 0 to 2; the broken line is independently the presence or absence of a bond; and the wavy line represents a cis- or trans-geometrical isomerism with respect to the double bond; a prodrug thereof, a pharmaceutically acceptable salt or solvate of them to a patient expected to enhance the expression of apoAI.
 2. The method according to claim 1, in which Ar¹ in formula (I) is a monocyclic or bicyclic aromatic heterocyclic group that may be optionally substituted, and that contains a nitrogen atom at the position adjacent to the constituent atom of the ring that has a binding bond.
 3. The method according to claim 1, in which Ar¹ in formula (I) is 2-pyridyl, 2-quinolyl, 2-quinoxalyl, 2-benzisoxazolyl, 2-benzothiazolyl, or 2-benzimidazolyl, each of which may be optionally substituted.
 4. The method according to any one of claims 1 to 3, in which Ar² in formula (I), which is condensed with ring B, is a benzene ring that may be optionally substituted, or a monocyclic aromatic heterocyclic group that may be optionally substituted.
 5. The method according to any one of claims 1 to 3, in which ring A in formula (I) is a phenyl that may be optionally substituted, or a monocyclic aromatic heterocyclic group that may be optionally substituted.
 6. The method according to claim 5, in which ring A in formula (I) is a phenyl or a monocyclic aromatic heterocyclic group, each of which may be optionally substituted, wherein the substituent is a halogen; a lower alkyl optionally substituted by a halogen or a lower alkoxy; a hydroxy; a lower alkoxy; phenoxy; naphthyloxy; an acyloxy; a carboxy; a lower alkoxycarbonyl; an amino optionally substituted by a lower alkyl or a lower acyl; a phenyl that may be optionally substituted by a lower alkoxy; a nitro; a lower alkylthio; a cyano; a monocyclic heterocyclic group; or an alkylenedioxy.
 7. The method according to any one of claims 1 to 3, in which Y¹ and/or Y² in formula (I) is a hydrogen.
 8. The method according to any one of claims 1 to 3, in which Z in formula (I) is oxygen.
 9. The method according to any one of claims 1 to 3, in which n in formula (I) is 1 or 2, and all of the broken line are the presence of a bond.
 10. The method according to claim 9, in which when n is 1 and the broken line is the presence of a bond, then the wavy line represents trans configuration with respect to the relationship between NRCZ and ring A, or alternatively when n is 2 and the broken lines are the presence of a bond, then the wavy line represents trans configuration with respect to the relationship between NRCZ and CY² and/or the relationship between CY¹ and ring A.
 11. A method of treatment or prevention of dyslipidemia or arteriosclerotic diseases, which comprises administrating a therapeutically effective amount of a compound of formula (I) as defined in claim 1, a prodrug thereof, a pharmaceutically acceptable salt or solvate of them to a patient suspected to have dyslipidemia or arteriosclerotic diseases. 12-17. (canceled)
 18. The method according to claim 4, in which Y¹ and/or Y² in formula (I) is a hydrogen.
 19. The method according to claim 5, in which Y¹ and/or Y² in formula (I) is a hydrogen.
 20. The method according to claim 6, in which Y¹ and/or Y² in formula (I) is a hydrogen.
 21. The method according to claim 4, in which Z in formula (I) is oxygen.
 22. The method according to claim 5, in which Z in formula (I) is oxygen.
 23. The method according to claim 6, in which Z in formula (I) is oxygen.
 24. The method according to claim 7, in which Z in formula (I) is oxygen.
 25. The method according to claim 4, in which n in formula (I) is 1 or 2, and all of the broken line are the presence of a bond.
 26. The method according to claim 5, in which n in formula (I) is 1 or 2, and all of the broken line are the presence of a bond.
 27. The method according to claim 6, in which n in formula (I) is 1 or 2, and all of the broken line are the presence of a bond.
 28. The method according to claim 7, in which n in formula (I) is 1 or 2, and all of the broken line are the presence of a bond.
 29. The method according to claim 8, in which n in formula (I) is 1 or 2, and all of the broken line are the presence of a bond. 